718 records
| MFID | Molecular factor | Category | Gene |
|---|---|---|---|
| MFID0505 | NC_000001.11:g.193213064_19325694del | copy number variation | CDC73 |
| MFID0506 | NC_000003.12:g.45217649_45221633del | copy number variation | CDCP1 |
| MFID0507 | NC_000016.10:g.82706957_82712663dul | copy number variation | CDH13 |
| MFID0508 | NC_000001.11:g.232154677_232164229dul | copy number variation | DISC1 |
| MFID0509 | LPA KIV-2 | copy number variation | LPA |
| MFID0510 | NC_000001.11:g.95164205_95170962dul | copy number variation | None |
| MFID0511 | NC_000012.12:g.18574942_18579403dul | copy number variation | PIK3C2G |
| MFID0512 | NC_000010.11:g.43623658_43625593dul | copy number variation | RET |
| MFID0513 | MBL2 LYQA secretor haplotype | haplotype | MBL2 |
| MFID0514 | ALOX5AP haplotype | haplotype | ALOX5AP |
| MFID0515 | NM_005141.5:c.[-455G>A;1433G>A;8558C>G] | haplotype | FGB |
| MFID0516 | LPA [PN;KIV-2] | haplotype | LPA |
| MFID0517 | NM_002203.4:c.[759C>T;873G>A] | haplotype | ITGA2 |
| MFID0518 | NM_003891.3:c.[-13A>G;-103G>A;-79G>A] | haplotype | PROZ |
| MFID0519 | NM_000024.6:c.[-47C>T;46G>A;79G>C] | haplotype | ADRB2 |
| MFID0520 | NM_000024.6:c.[46G>A;79G>C;491C>T] | haplotype | ADRB2 |
| MFID0521 | NC_000007.14:g.[87509329A>T;87509216A>C;87515500G>C;87501081C>T] | haplotype | ABCB1 |
| MFID0522 | NC_000004.12:g.[154604818C>T;154590745A>G] | haplotype | FGG|FGA |
| MFID0523 | NC_000009.12:g.[22096056A>G;22115027A>G;22119196T>C;22124478A>G;22125504G>C] | haplotype | CDKN2B-AS1 |
| MFID0524 | NC_000009.12:g.[22096056A>G;22115027A>G;22115960A>G;22124478A>G] | haplotype | CDKN2B-AS1 |
| MFID0525 | NM_004631.5:c.[1007-1082C>T;1007-1165A>G] | haplotype | LRP8 |
| MFID0526 | NC_000009.12:g.[22014138C>G;22018781T>A;22019674G>C;22024352C>T;22031006G>A] | haplotype | CDKN2B-AS1 |
| MFID0527 | NC_000010.10:g.[112835159A>G;112836503C>G;112837073C>G;112837538G>A;112838552C>G;112838892C>A;112839282T>A;112839579C>T;g.112839601C>A;113042093G>T] | haplotype | ADRA2A |
| MFID0528 | NM_002421.4:c.[-1607insG;-340T>C] | haplotype | MMP1 |
| MFID0529 | NC_000001.11:g.[55039995C>G;55039974G>A;55038977G>A;55030366T>C] | haplotype | PCSK9 |
| MFID0530 | NM_000078.3:c.[-2708G>A;-971A>G;-629A>C;118+279G>A;1264G>A] | haplotype | CETP |
| MFID0531 | NM_001437.3:c.[-789T>G;984G>A;*39G>A] | haplotype | ESR2 |
| MFID0532 | NC_000006.12:g.[46736602C>T;46735776A>G;46735073A>G;46716485C>T;46711566A>G;46709361C>A;46705206A>G] | haplotype | PLA2G7 |
| MFID0533 | NM_002052.3:c.[910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T;*1158C>T] | haplotype | GATA4 |
| MFID0534 | NC_000009.12:g.[22083405C>T;22098575A>G;22115960A>G;22125504G>C] | haplotype | CDKN2B-AS1 |
| MFID0535 | NC_000009.12:g.[22125504G>C;22124478A>G] | haplotype | None |
| MFID0536 | NM_005036.6:c.[-127+5156G>A;-127+7452C>A;-127+11398A>C] | haplotype | PPARA |
| MFID0537 | NM_001161352.2:c.[2027+37C>T;687C>T] | haplotype | KCNMA1 |
| MFID0538 | NM_000852.4:c.[313A>G;341C>T] | haplotype | GSTP1 |
| MFID0539 | NM_002052.3:c.[909+1970A>G;910-240C>T;946C>G;997+56C>A] | haplotype | GATA4 |
| MFID0540 | NM_002052.3:c.[909+1970A>G;910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T] | haplotype | GATA4 |
| MFID0541 | NM_002052.3:c.[909+1970A>G;910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T;*1158C>T] | haplotype | GATA4 |
| MFID0542 | NG_011963.2:g.[21351G>A;29482A>T;53431A>G;57503G>A] | haplotype | ALOX5AP |
| MFID0543 | NM_002421.4:c.[-1607insG;-519A>G;-340T>C] | haplotype | MMP1 |
| MFID0544 | NC_000003.12:g.[46357717G>A;46373456_46373487del] | haplotype | CCR2|CCR5 |
| MFID0545 | NM_001378373.1:c.[161G>A;170G>A;154C>T;-9-281C>A] | haplotype | MBL2 |
| MFID0546 | NM_030578.4:c.[*18G>A;-509C>T;29C>T] | haplotype | TGFB1 |
| MFID0547 | NM_000660.7:c.[-509C>T;29C>T;74G>C;788C>T] | haplotype | TGFB1 |
| MFID0548 | NM_000660.7:c.[-509C>T;29C>T] | haplotype | TGFB1 |
| MFID0549 | NM_001136.5:c.[-429T>C;-374T>A;244G>A] | haplotype | AGER |
| MFID0550 | NG_007279.1:g.[5077T>C;6042T>G] | haplotype | CD40 |
| MFID0551 | NM_001562.4:c.[-656G>T;-105C>T;-8-1360A>G;91+488G>C;361-221C>A;*183A>G] | haplotype | IL18 |
| MFID0552 | NM_001562.4:c.[-656G>T;-119A>C;-9+3005A>G;-8-919G>A;-8-372C>G;361-221C>A] | haplotype | IL18 |
| MFID0553 | NG_012575.2:g.[7219A>G;14934G>A;22218C>G] | haplotype | ACE2 |
| MFID0554 | NC_000017.11:g.[46896981T>C;46928464G>A;46931204G>A] | haplotype | GOSR2 |
| MFID0555 | NC_000006.12:g.[160442500T>C;160451754C>G;160486102C>T;160490021C>T;160493428A>G;160500534T>G;160519088A>G;160541471T>C;160548706C>G] | haplotype | SLC22A3|LPAL2|LPA |
| MFID0556 | NC_000006.12:g.[160442500T>C;160486102C>T;160541471T>C;160548706C>G] | haplotype | SLC22A3|LPAL2|LPA |
| MFID0557 | NC_000011.10:g.[14893764A>G;14888688A>G;14900334G>A] | haplotype | CYP2R1 |
| MFID0558 | NM_025144.4:c.[2608G>A;2746A>G] | haplotype | ALPK1 |
| MFID0559 | NC_000008.11:g.[58476006C>T;58500365A>C] | haplotype | CYP7A1 |
| MFID0560 | NM_000618.5:c.[64-1682G>A;220+10605T>C;221-164G>A;403-5895A>G] | haplotype | IGF1 |
| MFID0561 | NM_000618.5:c.[64-1682G>A;220+10605T>C;403-5895A>G;*2652T>C] | haplotype | IGF1 |
| MFID0562 | NM_000602.5:c.[-844A>G;506-451G>A;1088-106A>G] | haplotype | SERPINE1 |
| MFID0563 | NM_000602.5:c.[-844A>G;701-340G>A] | haplotype | SERPINE1 |
| MFID0564 | NM_001992.5:c.[-1738G>A;-506GGCCGCGGGAAGC[3];2860G>A;88+693C>A;88+6876C>A;88+7096C>T;*1468T>C]*NM_000600.5:c.[-174G>C;-572G>C;324+147C>G] | haplotype | F2R|IL6 |
| MFID0565 | NM_001992.5:c.[-1738G>A;2860G>A] | haplotype | F2R |
| MFID0566 | NM_000125.4:c.[453-397T>C;453-351A>G] | haplotype | ESR1 |
| MFID0567 | NM_000545.5:c.[1375C>T;1460T>C;1501+119G>T;*438A>G] | haplotype | HNF1A |
| MFID0568 | NM_000545.5:c.[1375C>T;1460T>C;1501+119G>T;*438A>G;452+136C>T] | haplotype | HNF1A |
| MFID0569 | NG_007932.1:g.[10733T>A;13661T>C;15254G>A] | haplotype | CYP4A11 |
| MFID0570 | NC_000001.11:g.[59907994A>C;59920071C>T;59923002G>A] | haplotype | CYP2J2 |
| MFID0571 | NM_001386809.1:c.[80-7C>T;368T>C;719-63G>T;*A>C] | haplotype | CXCL16 |
| MFID0572 | NM_002250.3:c.[820-60G>A;1049+78T>C;1120-487A>G] | haplotype | KCNN4 |
| MFID0573 | NM_000545.5:c.[327-2680C>T;327-1775A>G;1375C>T;1460T>C] | haplotype | HNF1A |
| MFID0574 | NM_000545.5:c.[327-2680C>T;327-1775A>G;1375C>T;1460T>C;1501+119G>T] | haplotype | HNF1A |
| MFID0575 | NM_000545.5:c.[327-2680C>T;327-1775A>G;1375C>T;1460T>C;1501+119G>T;*438A>G] | haplotype | HNF1A |
| MFID0576 | NM_000545.5:c.[327-2680C>T;327-1775A>G;1375C>T;1460T>C;1501+119G>T;*438A>G;452+136C>T] | haplotype | HNF1A |
| MFID0577 | NM_000545.5:c.[1460T>C;1501+119G>T;*438A>G;452+136C>T] | haplotype | HNF1A |
| MFID0578 | NM_000040.3:c.[-641C>A;-482C>T;-455T>C;1100C>T;*40G>C;3206C>G] | haplotype | APOC3 |
| MFID0579 | NM_002052.3:c.[909+1160C>T;909+1970A>G;910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T] | haplotype | GATA4 |
| MFID0580 | NM_002052.3:c.[909+1160C>T;909+1970A>G;910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T;*1158C>T] | haplotype | GATA4 |
| MFID0581 | NM_002052.3:c.[909+1160C>T;909+1970A>G;910-240C>T;946C>G;997+56C>A;1056C>T;1129A>G;*426C>T;*1158C>T;*1521C>G] | haplotype | GATA4 |
| MFID0582 | NM_000685.5:c.[-1106A>T;-48+59A>G;-47-11020G>A;573C>T;*86A>C;*798G>A] | haplotype | AGTR1 |
| MFID0583 | NC_000005.10:g.[60174072G>A;60365629A>G;60206693A>G;60298071A>G;60304214G>C;60354709A>G] | haplotype | PDE4D |
| MFID0584 | NC_000001.11:g.[222614720C>T;g.222617024G>A;222625623G>A;222633671C>T;222650187A>C;222658030A>G;222658668A>G;222661880A>C;222666496A>G] | haplotype | MIA3 |
| MFID0585 | NM_001082.5:c.[344-979T>A;919-446C>T;1297G>A] | haplotype | CYP4F2 |
| MFID0586 | NM_173841.3:c.[62+732G>A;117T>C;214+94T>G;399T>C;483+1061G>A] | haplotype | IL1RN |
| MFID0587 | NM_000237.3:c.[1421C>G;106G>A;953A>G] | haplotype | LPL |
| MFID0588 | NM_002422.5:c.[-1612dup;-376C>G;1161G>A] | haplotype | MMP3 |
| MFID0589 | NM_000106.6:c.[775del;506-1G>A;100C>T] | haplotype | CYP2D6 |
| MFID0590 | NM_002052.3:c.[1056C>T;1129A>G;*426C>T;*1158C>T;*1521C>G] | haplotype | GATA4 |
| MFID0591 | NM_003326.5:c.[203-288A>G;202+119A>G;154-5804T>C;154-8539T>C] | haplotype | TNFSF4 |
| MFID0592 | NM_004994.3:c.[-1562C>T;836A>G] | haplotype | MMP9 |
| MFID0593 | NM_000769.4:c.[681G>A;636G>A] | haplotype | CYP2C19 |
| MFID0594 | NM_000769.4:c.[681G>A;636G>A;-806C>T] | haplotype | CYP2C19 |
| MFID0595 | NM_000041.4:c.[-491A>T;388T>C] | haplotype | APOE |
| MFID0596 | NM_001629.4:c.[70+18C>A;170+105T>A] | haplotype | ALOX5AP |
| MFID0597 | NM_000576.3:c.[-3737C>T;-1468G>C;-511C>T] | haplotype | IL1B |
| MFID0598 | NC_000005.10:g.[4022536T>C;4029676C>T;4035819G>A] | haplotype | None |
| MFID0599 | NM_138554.5:c.[896A>G;1196C>T] | haplotype | TLR4 |
| MFID0600 | NM_019616.4:c.[-670A>C;-323del;-122T>C;1172G>A] | haplotype | F7 |
| MFID0601 | NM_000040.3:c.[*40G>C;-455T>C;-482C>T] | haplotype | APOC3 |
| MFID0602 | NG_012100.1:g.[4295A>G;7762G>C;13685G>C;14446T>C] | haplotype | MMP3 |
| MFID0603 | NM_000961.4:c.[*2479T>C;1117C>A;252C>T] | haplotype | PTGIS |
| MFID0604 | NC_000019.10:g.[8311547G>A;49505441A>G;49510639T>C;49517245G>A;49524145C>G;49536138A>G;48177784G>A] | haplotype | PTGIS |
| MFID0605 | NC_000023.11:g.[129656490A>G;129655744A>C;129653796C>T;129651324C>T;129648585G>T;129648435G>C;129652326T>C;129646415G>C] | haplotype | APLN |
| MFID0606 | NM_002052.3:c.[946C>G;997+56C>A;1056C>T;1129A>G;*426C>T] | haplotype | GATA4 |
| MFID0607 | NM_000173.7:c.[482C>T;-5T>C] | haplotype | GP1BA |
| MFID0608 | NM_000602.5:c.[43G>A;*722T>G] | haplotype | SERPINE1 |
| MFID0609 | NM_002575.3:c.[358A>G;1212C>G;1238C>G] | haplotype | SERPINB2 |
| MFID0610 | NM_003005.4:c.[992G>A;1807G>A;1918G>T;2266A>C;2346G>T;2346G>T] | haplotype | SELP |
| MFID0611 | NC_000002.12:g.[21008652G>A;21014914T>G;21021486T>G;21022457G>T;21003688A>G] | haplotype | APOB |
| MFID0612 | NM_003376.6:c.[-2578A>C;-94C>G;*237C>T] | haplotype | VEGFA |
| MFID0613 | NM_003376.6:c.[-2578A>C;-460C>T;-94C>G] | haplotype | VEGFA |
| MFID0614 | NM_000583.4:c.[1296T>G;1307C>A] | haplotype | GC |
| MFID0615 | NM_012238.5:c.[943-3428C>G;1090+207A>G;*480C>T] | haplotype | SIRT1 |
| MFID0616 | NM_000956.4:c.[-12813G>A;-10250T>A;-6179A>G] | haplotype | PTGER2 |
| MFID0617 | NM_001972.4:c.[-761G>A;4890C>A] | haplotype | ELANE |
| MFID0618 | NM_000545.5:c.[327-1775A>G;1375C>T;1460T>C;1501+119G>T] | haplotype | HNF1A |
| MFID0619 | NM_000545.5:c.[327-1775A>G;1375C>T;1460T>C;1501+119G>T;*438A>G] | haplotype | HNF1A |
| MFID0620 | NM_000041.4:c.[526C>T;388T>C] | haplotype | APOE |
| MFID0621 | NM_004631.5:c.[1007-1165A>G;1257C>A;2622C>T;2855G>A] | haplotype | LRP8 |
| MFID0622 | NC_000014.9:g.[35225975T>A;35258383G>A;35292469C>G;35303372A>G;35340878A>G] | haplotype | PRORP|PSMA6 |
| MFID0623 | NM_020469.3:c.[796C>A;526C>G] | haplotype | ABO |
| MFID0624 | NM_004797.4:c.[-4033C>A;-11377C>G;-11391G>A;-3971A>G;45T>G;214+62G>T] | haplotype | ADIPOQ |
| MFID0625 | NG_032899.2:g.[9781A>G;9859C>G] | haplotype | PROCR |
| MFID0626 | NC_000012.12:g.[SG12S16A>G;96007474G>A;96009832T>C;96015423A>G; 96020673T>C;96028599T>C;96032219T>G;96041102C>T;96044775G>A;96047515G>A] | haplotype | LTA4H |
| MFID0627 | NC_000001.11:g.[173206693A>G;173208097C>T] | haplotype | TNFSF4 |
| MFID0628 | NM_000295.5:c.[710T>C;1096G>A] | haplotype | SERPINA1 |
| MFID0629 | NM_000442.5:c.[373G>C;1688G>A;2008A>G] | haplotype | PECAM1 |
| MFID0630 | NM_000745.3:c.[107-1865T>C;1192G>A] | haplotype | CHRNA5 |
| MFID0631 | ALOX5, VARIANT PROMOTER SP1 BINDING | insertion and deletion | ALOX5 |
| MFID0632 | APOB 3'VNTR | insertion and deletion | APOB |
| MFID0633 | GP1BA VNTR | insertion and deletion | GP1BA |
| MFID0634 | NC_000004.12:g.3525052_3532208del | insertion and deletion | LRPAP1 |
| MFID0635 | NC_000011.10:g.236380_236381insCCCGCGGCGCCCCA | insertion and deletion | SIRT3 |
| MFID0636 | NC_000019.10:g.38900888_91delTAAA | insertion and deletion | SIRT2 |
| MFID0637 | NG_011747.2:g.3628_3670dup | insertion and deletion | SLC6A4 |
| MFID0638 | NG_050628.1:g.4670ATTG[1] | insertion and deletion | NFKB1 |
| MFID0639 | NM_000106.6:c.dup | insertion and deletion | CYP2D6 |
| MFID0640 | NM_000209.4:c.-108dupG | insertion and deletion | PDX1 |
| MFID0641 | NM_000384.3:c.26TGGCGCTGC[1] | insertion and deletion | APOB |
| MFID0642 | NM_000603.5:c.582+290_582+343del | insertion and deletion | NOS3 |
| MFID0643 | NM_000618.5:-841CA[n] | insertion and deletion | IGF1 |
| MFID0644 | NM_000682.7:c.893_900dup | insertion and deletion | ADRA2B |
| MFID0645 | NM_000789.4:c.2306-105_2306-104insTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | insertion and deletion | ACE |
| MFID0646 | NM_000789.4:c.4656CT[2] | insertion and deletion | ACE |
| MFID0647 | NM_002422.5:c.-1612dup | insertion and deletion | MMP3 |
| MFID0648 | NM_003006.4:c.9583_12000dul | insertion and deletion | SELPLG |
| MFID0649 | NM_003998.4:c.-94delATTG | insertion and deletion | NFKB1 |
| MFID0650 | NM_015120.4:c.73466485_73466720dupGAG | insertion and deletion | ALMS1 |
| MFID0651 | NM_019101.3:c.-724del | insertion and deletion | APOM |
| MFID0652 | NM_019616.4:c.-323insCCTATATCCT | insertion and deletion | F7 |
| MFID0653 | NM_145899.3:c.136-15_136-14del | insertion and deletion | HMGA1 |
| MFID0654 | PLAT 311bp ins/del | insertion and deletion | PLAT |
| MFID0655 | mtDNA haplogroup H | other | None |
| MFID0656 | C4B*Q0 | other | C4B |
| MFID0657 | CYP2D6 frequency | other | CYP2D6 |
| MFID0658 | GSTM1 null genotype | other | GSTM1 |
| MFID0659 | GSTT1 null genotype | other | GSTT1 |
| MFID0660 | HLA-DRB1*01 | other | HLA-DRB1 |
| MFID0661 | HP genotype | other | HP |
| MFID0662 | TRBJ2-1 frequency | other | TRBJ2-1 |
| MFID0663 | TRBV12-3 frequency | other | TRBV12-3 |
| MFID0664 | TRBV2 frequency | other | TRBV2 |
| MFID0665 | TRBV29-1 frequency | other | TRBV29-1 |
| MFID0666 | TRBV30 frequency | other | TRBV30 |
| MFID0667 | HLA-DQA1*02 | other | HLA-DRB1 |
| MFID0668 | HLA-DRB1*0101 | other | HLA-DRB1 |
| MFID0669 | HLA-DRB1*07 | other | HLA-DRB1 |
| MFID0670 | APOB PvuII | single nucleotide variant | APOB |
| MFID0671 | chrY HindIII | single nucleotide variant | None |
| MFID0672 | FGB_BclI | single nucleotide variant | FGB |
| MFID0673 | LPA PN | single nucleotide variant | LPA |
| MFID0674 | NC_000001.11:g.109279544G>A | single nucleotide variant | PSRC1 |
| MFID0675 | NC_000001.11:g.158880164C>G | single nucleotide variant | None |
| MFID0676 | NC_000001.11:g.173208097C>T | single nucleotide variant | TNFSF4 |
| MFID0677 | NC_000001.11:g.190092815A>T | single nucleotide variant | BRINP3 |
| MFID0678 | NC_000001.11:g.190139751C>T | single nucleotide variant | BRINP3 |
| MFID0679 | NC_000001.11:g.190186503C>T | single nucleotide variant | BRINP3 |
| MFID0680 | NC_000001.11:g.190194864T>G | single nucleotide variant | BRINP3 |
| MFID0681 | NC_000001.11:g.190202510G>C | single nucleotide variant | BRINP3 |
| MFID0682 | NC_000001.11:g.190290531T>C | single nucleotide variant | BRINP3 |
| MFID0683 | NC_000001.11:g.190382547C>T | single nucleotide variant | BRINP3 |
| MFID0684 | NC_000001.11:g.190458964A>T | single nucleotide variant | BRINP3 |
| MFID0685 | NC_000001.11:g.190471407T>C | single nucleotide variant | BRINP3 |
| MFID0686 | NC_000001.11:g.190491143G>A | single nucleotide variant | BRINP3 |
| MFID0687 | NC_000001.11:g.32862564G>A | single nucleotide variant | FNDC5 |
| MFID0688 | NC_000001.11:g.55030366T>C | single nucleotide variant | PCSK9 |
| MFID0689 | NC_000001.11:g.59896030A>T | single nucleotide variant | CYP2J2 |
| MFID0690 | NC_000001.11:g.59896449T>C | single nucleotide variant | CYP2J2 |
| MFID0691 | NC_000001.11:g.59907994A>C | single nucleotide variant | CYP2J2 |
| MFID0692 | NC_000002.12:g.112833698A>G | single nucleotide variant | IL1B |
| MFID0693 | NC_000002.12:g.112835941G>A | single nucleotide variant | IL1B |
| MFID0694 | NC_000002.12:g.21008652G>A | single nucleotide variant | APOB |
| MFID0695 | NC_000002.12:g.238253316C>T | single nucleotide variant | PER2 |
| MFID0696 | NC_000002.12:g.73331275G>A | single nucleotide variant | ALMS1 |
| MFID0697 | NC_000003.12:g.38592432G>C | single nucleotide variant | SCN5A |
| MFID0698 | NC_000003.12:g.38736063T>G | single nucleotide variant | SCN10A |
| MFID0699 | NC_000004.12:g.177339718C>T | single nucleotide variant | NEIL3 |
| MFID0700 | NC_000004.12:g.55502504G>A | single nucleotide variant | CLOCK |
| MFID0701 | NC_000005.10:g.4022536T>C | single nucleotide variant | None |
| MFID0702 | NC_000005.10:g.4029676C>T | single nucleotide variant | None |
| MFID0703 | NC_000005.10:g.4035819G>A | single nucleotide variant | None |
| MFID0704 | NM_147686.4:c.28G>A | single nucleotide variant | TRAF3IP2 |
| MFID0705 | NC_000006.12:g.13573450A>G | single nucleotide variant | SIRT5 |
| MFID0706 | NC_000006.12:g.13574110G>A | single nucleotide variant | SIRT5 |
| MFID0707 | NC_000006.12:g.13574131C>A | single nucleotide variant | SIRT5 |
| MFID0708 | NC_000006.12:g.13574259G>C | single nucleotide variant | SIRT5 |
| MFID0709 | NC_000006.12:g.13574287G>C | single nucleotide variant | SIRT5 |
| MFID0710 | NC_000006.12:g.160493428A>G | single nucleotide variant | LPAL2 |
| MFID0711 | NC_000006.12:g.160589086A>G | single nucleotide variant | LPA |
| MFID0712 | NC_000006.12:g.26458037T>C | single nucleotide variant | BTN2A1 |
| MFID0713 | NC_000006.12:g.31730180C>G | single nucleotide variant | DDAH2 |
| MFID0714 | NC_000006.12:g.46736602C>T | single nucleotide variant | PLA2G7 |
| MFID0715 | NC_000007.14:g.106285307C>T | single nucleotide variant | NAMPT |
| MFID0716 | NC_000007.14:g.137004249T>C | single nucleotide variant | CHRM2 |
| MFID0717 | NC_000007.14:g.19013110G>A | single nucleotide variant | HDAC9 |
| MFID0718 | NC_000007.14:g.86763295C>A | single nucleotide variant | GRM3 |
| MFID0719 | NC_000007.14:g.87509329A>G | single nucleotide variant | VAMP8 |
| MFID0720 | NC_000008.11:g.41302340C>T | single nucleotide variant | SFRP1 |
| MFID0721 | NC_000009.12:g.136670698A>G | single nucleotide variant | MIR126 |
| MFID0722 | NC_000009.12:g.22003368G>A | single nucleotide variant | CDKN2B |
| MFID0723 | NC_000009.12:g.22031006G>A | single nucleotide variant | CDKN2B-AS1 |
| MFID0724 | NC_000009.12:g.22061615C>T | single nucleotide variant | CDKN2B-AS1 |
| MFID0725 | NC_000009.12:g.22067594A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0726 | NC_000009.12:g.22072302G>C | single nucleotide variant | CDKN2B-AS1 |
| MFID0727 | NC_000009.12:g.22081398G>T | single nucleotide variant | CDKN2B-AS1 |
| MFID0728 | NC_000009.12:g.22081851C>T | single nucleotide variant | CDKN2B-AS1 |
| MFID0729 | NC_000009.12:g.22083405C>T | single nucleotide variant | CDKN2B-AS1 |
| MFID0730 | NC_000009.12:g.22087474T>C | single nucleotide variant | CDKN2B-AS1 |
| MFID0731 | NC_000009.12:g.22096056A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0732 | NC_000009.12:g.22098575A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0733 | NC_000009.12:g.22098620A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0734 | NC_000009.12:g.22103814A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0735 | NC_000009.12:g.22115027A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0736 | NC_000009.12:g.22115960A>G | single nucleotide variant | CDKN2B-AS1 |
| MFID0737 | NC_000009.12:g.22119196T>C | single nucleotide variant | CDKN2B-AS1 |
| MFID0738 | NC_000009.12:g.22124478A>G | single nucleotide variant | None |
| MFID0739 | NC_000009.12:g.22125504G>C | single nucleotide variant | None |
| MFID0740 | NC_000009.12:g.22140225A>C | single nucleotide variant | None |
| MFID0741 | NC_000010.11:g.111282335T>G | single nucleotide variant | ADRA2A |
| MFID0742 | NC_000010.11:g.44258419A>G | single nucleotide variant | CXCL12 |
| MFID0743 | NC_000010.11:g.44280376C>T | single nucleotide variant | CXCL12 |
| MFID0744 | NC_000010.11:g.51299646A>G | single nucleotide variant | MIR605 |
| MFID0745 | NC_000010.11:g.89243170C>T | single nucleotide variant | LIPA |
| MFID0746 | NC_000010.11:g.89246097C>T | single nucleotide variant | LIPA |
| MFID0747 | NC_000011.10:g.102799765C>G | single nucleotide variant | MMP1 |
| MFID0748 | NC_000011.10:g.105029761G>A | single nucleotide variant | CASP1 |
| MFID0749 | NC_000011.10:g.116736721C>T | single nucleotide variant | APOA5 |
| MFID0750 | NC_000011.10:g.116793324G>A | single nucleotide variant | APOA5 |
| MFID0751 | NC_000011.10:g.17428382C>T | single nucleotide variant | KCNJ5 |
| MFID0752 | NC_000011.10:g.236370C>G | single nucleotide variant | SIRT3 |
| MFID0753 | NC_000011.10:g.236473C>T | single nucleotide variant | SIRT3 |
| MFID0754 | NC_000011.10:g.45856137C>G | single nucleotide variant | CRY2 |
| MFID0755 | NC_000011.10:g.57236870G>T | single nucleotide variant | APLNR |
| MFID0756 | NC_000012.12:g.10986253C>T | single nucleotide variant | TAS2R50 |
| MFID0757 | NC_000012.12:g.12148964C>T | single nucleotide variant | LRP6 |
| MFID0758 | NC_000012.12:g.47838310C>T | single nucleotide variant | VDR |
| MFID0759 | NC_000012.12:g.49853685G>A | single nucleotide variant | FAIM2 |
| MFID0760 | NC_000013.11:g.28399484G>A | single nucleotide variant | FLT1 |
| MFID0761 | NC_000014.9:g.55112795A>G | single nucleotide variant | LGALS3 |
| MFID0762 | NC_000014.9:g.55147918C>T | single nucleotide variant | LGALS3 |
| MFID0763 | NC_000016.10:g.53767042T>G | single nucleotide variant | FTO |
| MFID0764 | NC_000017.11:g.40514261A>G | single nucleotide variant | CCR7 |
| MFID0765 | NM_023079.5:c.390+355C>T | single nucleotide variant | UBE2Z |
| MFID0766 | NC_000017.11:g.75569090A>G | single nucleotide variant | LLGL2 |
| MFID0767 | NC_000019.10:g.11617987A>G | single nucleotide variant | ZNF627 |
| MFID0768 | NC_000019.10:g.15476534T>C | single nucleotide variant | PGLYRP2 |
| MFID0769 | NM_001082.5:c.1297G>A | single nucleotide variant | CYP4F2 |
| MFID0770 | NC_000019.10:g.2160530C>A | single nucleotide variant | AP3D1|DOT1L|SF3A2 |
| MFID0771 | NC_000019.10:g.38899853C>T | single nucleotide variant | SIRT2 |
| MFID0772 | NC_000019.10:g.38900270A>G | single nucleotide variant | SIRT2 |
| MFID0773 | NC_000019.10:g.41302527A>T | single nucleotide variant | HNRNPUL1 |
| MFID0774 | NC_000021.9:g.26845001C>G | single nucleotide variant | ADAMTS1 |
| MFID0775 | NC_000023.11:g.129651324C>T | single nucleotide variant | APLN |
| MFID0776 | NC_000023.11:g.129652326T>C | single nucleotide variant | APLN |
| MFID0777 | NC_000023.11:g.129656490A>G | single nucleotide variant | APLN |
| MFID0778 | NC_012920.1:m.5178C>A | single nucleotide variant | MT-ND2 |
| MFID0779 | NG_007086.2:g.4195G>T | single nucleotide variant | ARG1 |
| MFID0780 | NG_007291.1:g.12721G>A | single nucleotide variant | CYBA |
| MFID0781 | NG_007556.1:g.15165C>G | single nucleotide variant | TNNT2 |
| MFID0782 | NG_007570.2:g.18060G>A | single nucleotide variant | IFNGR2 |
| MFID0783 | NG_007931.1:g.4930G>T | single nucleotide variant | CYP2J2 |
| MFID0784 | NG_007972.1:g.37394C>T | single nucleotide variant | CYP2C8 |
| MFID0785 | NG_008422.2:g.210863T>G | single nucleotide variant | TBXAS1 |
| MFID0786 | NG_008845.2:g.42446C>T | single nucleotide variant | FXN |
| MFID0787 | NG_009369.2:g.4982G>A | single nucleotide variant | GJA5 |
| MFID0788 | NG_011437.1:g.4543T>C | single nucleotide variant | ALOX5 |
| MFID0789 | NG_011475.2:g.8374A>G | single nucleotide variant | TLR4 |
| MFID0790 | NG_011690.1:g.2043G>A | single nucleotide variant | ALMS1 |
| MFID0791 | NG_011963.2:g.29482A>T | single nucleotide variant | ALOX5AP |
| MFID0792 | NG_011963.2:g.49933A>C | single nucleotide variant | ALOX5AP |
| MFID0793 | NG_011963.2:g.57503G>A | single nucleotide variant | ALOX5AP |
| MFID0794 | NG_012020.1:g.4714G>C | single nucleotide variant | ADRA2A |
| MFID0795 | NG_012027.1:g.4959G>A | single nucleotide variant | THBD |
| MFID0796 | NG_012110.1:g.12147G>A | single nucleotide variant | PDCD1 |
| MFID0797 | NG_012213.1:g.2713T>G | single nucleotide variant | SOD3 |
| MFID0798 | NG_012344.1:g.5713T>A | single nucleotide variant | NFKBIL1 |
| MFID0799 | NG_012575.2:g.22218C>G | single nucleotide variant | ACE2 |
| MFID0800 | NG_012575.2:g.7219A>G | single nucleotide variant | ACE2 |
| MFID0801 | NG_012969.1:g.87653T>A | single nucleotide variant | FTO |
| MFID0802 | NG_013007.1:g.6289C>T | single nucleotide variant | CRP |
| MFID0803 | NG_016621.2:g.10376C>T | single nucleotide variant | MIAT |
| MFID0804 | NG_016621.2:g.4063T>C | single nucleotide variant | MIAT |
| MFID0805 | NG_016621.2:g.4137T>C | single nucleotide variant | MIAT |
| MFID0806 | NG_016757.1:g.64135C>T | single nucleotide variant | CLEC16A |
| MFID0807 | NG_021140.1:g.21665G>A | single nucleotide variant | ADIPOQ-AS1 |
| MFID0808 | NG_021159.1:g.405T>A | single nucleotide variant | GHSR |
| MFID0809 | NG_027957.2:g.322637T>C | single nucleotide variant | PDE4D |
| MFID0810 | NG_029220.1:g.30226T>C | single nucleotide variant | ILF3 |
| MFID0811 | NG_032121.1:g.9267C>G | single nucleotide variant | TCF21 |
| MFID0812 | NG_032650.1:g.20120A>G | single nucleotide variant | MTAP |
| MFID0813 | NG_032899.2:g.9781A>G | single nucleotide variant | PROCR |
| MFID0814 | NG_032899.2:g.9859C>G | single nucleotide variant | PROCR |
| MFID0815 | NG_032906.1:g.21257A>T | single nucleotide variant | F2R |
| MFID0816 | NG_033929.1:g.129835C>G | single nucleotide variant | ROS1 |
| MFID0817 | NG_046344.1:g.106140A>C | single nucleotide variant | COL13A1 |
| MFID0818 | NG_047153.1:g.3915T>C | single nucleotide variant | SIRT6 |
| MFID0819 | NG_047153.1:g.4658C>A | single nucleotide variant | SIRT6 |
| MFID0820 | NM_000024.6:c.46G>A | single nucleotide variant | ADRB2 |
| MFID0821 | NM_000024.6:c.-47C>T | single nucleotide variant | ADRB2 |
| MFID0822 | NM_000024.6:c.491C>T | single nucleotide variant | ADRB2 |
| MFID0823 | NM_000024.6:c.79G>C | single nucleotide variant | ADRB2 |
| MFID0824 | NM_000025.3:c.190T>C | single nucleotide variant | ADRB3 |
| MFID0825 | NM_000036.3:c.34C>T | single nucleotide variant | AMPD1 |
| MFID0826 | NM_000039.3:c.-21+67C>T | single nucleotide variant | APOA1 |
| MFID0827 | NM_000039.3:c.-21+68G>A | single nucleotide variant | APOA1 |
| MFID0828 | NM_000039.3:c.43+41T>C | single nucleotide variant | APOA1 |
| MFID0829 | NM_000040.3:c.*40G>C | single nucleotide variant | APOC3 |
| MFID0830 | NM_000041.4:c.-219G>T | single nucleotide variant | APOE |
| MFID0831 | NM_000041.4:c.388T>C | single nucleotide variant | APOE |
| MFID0832 | NM_000041.4:c.526C>T | single nucleotide variant | APOE |
| MFID0833 | NM_000043.6:c.-670G>A | single nucleotide variant | FAS |
| MFID0834 | NM_000064.4:c.364C>G | single nucleotide variant | C3 |
| MFID0835 | NM_000078.3:c.118+279G>A | single nucleotide variant | CETP |
| MFID0836 | NM_000078.3:c.1264G>A | single nucleotide variant | CETP |
| MFID0837 | NM_000078.3:c.-629C>A | single nucleotide variant | CETP |
| MFID0838 | NM_000101.4:c.214T>C | single nucleotide variant | CYBA |
| MFID0839 | NM_000125.4:c.453-351A>G | single nucleotide variant | ESR1 |
| MFID0840 | NM_000125.4:c.453-397T>C | single nucleotide variant | ESR1 |
| MFID0841 | NM_000129.4:c.103G>T | single nucleotide variant | F13A1 |
| MFID0842 | NM_000130.5:c.1601G>A | single nucleotide variant | F5 |
| MFID0843 | NM_000130.5:c.2401C>T | single nucleotide variant | F5 |
| MFID0844 | NM_000134.4:c.163A>G | single nucleotide variant | FABP2 |
| MFID0845 | NM_000144.5:c.384+4857G>A | single nucleotide variant | FXN |
| MFID0846 | NM_000173.7:c.482C>T | single nucleotide variant | GP1BA |
| MFID0847 | NM_000186.4:c.1204C>T | single nucleotide variant | CFH |
| MFID0848 | NM_000201.3:c.1405A>G | single nucleotide variant | ICAM1 |
| MFID0849 | NM_000208.4:c.1650G>A | single nucleotide variant | INSR |
| MFID0850 | NM_000212.3:c.176T>C | single nucleotide variant | ITGB3 |
| MFID0851 | NM_000230.3:c.-2548G>A | single nucleotide variant | LEP |
| MFID0852 | NM_000234.3:c.-7C>T | single nucleotide variant | LIG1 |
| MFID0853 | NM_000236.3:c.-514C>T | single nucleotide variant | LIPC |
| MFID0854 | NM_000237.3:c.106G>A | single nucleotide variant | LPL |
| MFID0855 | NM_000237.3:c.1322+483T>A | single nucleotide variant | LPL |
| MFID0856 | NM_000237.3:c.1421C>G | single nucleotide variant | LPL |
| MFID0857 | NM_000237.3:c.776-172G>A | single nucleotide variant | LPL |
| MFID0858 | NM_000238.4:c.2690A>C | single nucleotide variant | KCNH2 |
| MFID0859 | NM_000243.3:c.2080A>G | single nucleotide variant | MEFV |
| MFID0860 | NM_000246.4:c.-168A>G | single nucleotide variant | CIITA |
| MFID0861 | NM_000250.2:c.-129G>A | single nucleotide variant | MPO |
| MFID0862 | NM_000295.5:c.1096G>A | single nucleotide variant | SERPINA1 |
| MFID0863 | NM_000305.3:c.443C>G | single nucleotide variant | PON2 |
| MFID0864 | NM_000305.3:c.932C>G | single nucleotide variant | PON2 |
| MFID0865 | NM_000331.6:c.288T>C | single nucleotide variant | SAA1 |
| MFID0866 | NM_000361.3:c.1418C>T | single nucleotide variant | THBD |
| MFID0867 | NM_000376.3:c.1024+283G>T | single nucleotide variant | VDR |
| MFID0868 | NM_000384.3:c.12541G>T | single nucleotide variant | APOB |
| MFID0869 | NM_000384.3:c.7545C>T | single nucleotide variant | APOB |
| MFID0870 | NM_000388.4:c.1378-1412A>G | single nucleotide variant | CASR |
| MFID0871 | NM_000388.4:c.2956G>T | single nucleotide variant | CASR |
| MFID0872 | NM_000410.4:c.845G>A | single nucleotide variant | HFE |
| MFID0873 | NM_000418.4:c.223A>G | single nucleotide variant | IL4R |
| MFID0874 | NM_000419.5:c.2621T>G | single nucleotide variant | ITGA2B |
| MFID0875 | NM_000442.5:c.1688G>A | single nucleotide variant | PECAM1 |
| MFID0876 | NM_000442.5:c.2008A>G | single nucleotide variant | PECAM1 |
| MFID0877 | NM_000442.5:c.373G>C | single nucleotide variant | PECAM1 |
| MFID0878 | NM_000446.7:c.-108C>T | single nucleotide variant | PON1 |
| MFID0879 | NM_000446.7:c.163T>A | single nucleotide variant | PON1 |
| MFID0880 | NM_000446.7:c.575A>G | single nucleotide variant | PON1 |
| MFID0881 | NM_000450.2:c.445A>C | single nucleotide variant | SELE |
| MFID0882 | NM_000450.2:c.98G>T | single nucleotide variant | SELE |
| MFID0883 | NM_000460.4:c.5709A>G | single nucleotide variant | TPO |
| MFID0884 | NM_000460.4:c.5713A>G | single nucleotide variant | THPO |
| MFID0885 | NM_000488.4:c.1246G>T | single nucleotide variant | SERPINC1 |
| MFID0886 | NM_000505.4:c.-4T>C | single nucleotide variant | F12 |
| MFID0887 | NM_000506.5:c.*97G>A | single nucleotide variant | F2 |
| MFID0888 | NM_000506.5:c.494C>T | single nucleotide variant | F2 |
| MFID0889 | NM_000527.5:c. | single nucleotide variant | LDLR |
| MFID0890 | NM_000545.8:c.1375C>T | single nucleotide variant | HNF1A |
| MFID0891 | NM_000545.8:c.1460G>A | single nucleotide variant | HNF1A |
| MFID0892 | NM_000545.8:c.1501+119G>T | single nucleotide variant | HNF1A |
| MFID0893 | NM_000552.5:c.7682T>A | single nucleotide variant | VWF |
| MFID0894 | NM_000552.5:c.7729+252A>T | single nucleotide variant | VWF |
| MFID0895 | NM_000567.3:c.552G>C | single nucleotide variant | CRP |
| MFID0896 | NM_000567.3:c.-717A>G | single nucleotide variant | CRP |
| MFID0897 | NM_000572.3:c.-1082A>G | single nucleotide variant | IL10 |
| MFID0898 | NM_000576.3:c.-1468G>C | single nucleotide variant | IL1B |
| MFID0899 | NM_000576.3:c.315C>T | single nucleotide variant | IL1B |
| MFID0900 | NM_000576.3:c.-3737C>T | single nucleotide variant | IL1B |
| MFID0901 | NM_000576.3:c.-511C>T | single nucleotide variant | IL1B |
| MFID0902 | NM_000579.4:c.-301+246A>G | single nucleotide variant | CCR5 |
| MFID0903 | NM_000589.4:c.-589C>T | single nucleotide variant | IL4 |
| MFID0904 | NM_000591.4:c.-260C>T | single nucleotide variant | CD14 |
| MFID0905 | NM_000594.3:c.-488G>A | single nucleotide variant | TNF |
| MFID0906 | NM_000594.4:c.-1031T>C | single nucleotide variant | TNF |
| MFID0907 | NM_000594.4:c.-863C>A | single nucleotide variant | TNF |
| MFID0908 | NM_000595.4:c.-10+90A>G | single nucleotide variant | LTA |
| MFID0909 | NM_000595.4:c.-162G>A | single nucleotide variant | LTA |
| MFID0910 | NM_000595.4:c.179C>A | single nucleotide variant | LTA |
| MFID0911 | NM_000600.5:c.-174G>C | single nucleotide variant | IL6 |
| MFID0912 | NM_000600.5:c.-572G>C | single nucleotide variant | IL6 |
| MFID0913 | NM_000600.5:c.-598G>A | single nucleotide variant | IL6 |
| MFID0914 | NM_000602.5:c.*722T>G | single nucleotide variant | SERPINE1 |
| MFID0915 | NM_000602.5:c.-675A>G | single nucleotide variant | SERPINE1 |
| MFID0916 | NM_000603.5:c.-51-762C>T | single nucleotide variant | NOS3 |
| MFID0917 | NM_000603.5:c.894T>G | single nucleotide variant | NOS3 |
| MFID0918 | NM_000619.3:c.+874T>A | single nucleotide variant | IFNG |
| MFID0919 | NM_000621.5:c.102C>T | single nucleotide variant | HTR2A |
| MFID0920 | NM_000623.4:c.-58T>C | single nucleotide variant | BDKRB2 |
| MFID0921 | NM_000636.4:c.47T>C | single nucleotide variant | SOD2 |
| MFID0922 | NM_000660.7:c.29C>T | single nucleotide variant | TGFB1 |
| MFID0923 | NM_000660.7:c.-509C>T | single nucleotide variant | TGFB1 |
| MFID0924 | NM_000660.7:c.74G>C | single nucleotide variant | TGFB1 |
| MFID0925 | NM_000660.7:c.788C>T | single nucleotide variant | TGFB1 |
| MFID0926 | NM_000669.5:c.1048A>G | single nucleotide variant | ADH1C |
| MFID0927 | NM_000684.3:c.1165G>C | single nucleotide variant | ADRB1 |
| MFID0928 | NM_000684.3:c.145A>G | single nucleotide variant | ADRB1 |
| MFID0929 | NM_000685.5:c.*86A>C | single nucleotide variant | AGTR1 |
| MFID0930 | NM_000685.5:c.573C>T | single nucleotide variant | AGTR1 |
| MFID0931 | NM_000685.5:c.-810T>A | single nucleotide variant | AGTR1 |
| MFID0932 | NM_000686.5:c.3123C>A | single nucleotide variant | AGTR2 |
| MFID0933 | NM_000690.4:c.1510G>A | single nucleotide variant | ALDH2 |
| MFID0934 | NM_000745.3:c.1192G>A | single nucleotide variant | CHRNA5 |
| MFID0935 | NM_000754.4:c.472G>A | single nucleotide variant | COMT |
| MFID0936 | NM_000761.5:c.-9-154C>A | single nucleotide variant | CYP1A2 |
| MFID0937 | NM_000769.4:c.681G>A | single nucleotide variant | CYP2C19 |
| MFID0938 | NM_000769.4:c.-806C>T | single nucleotide variant | CYP2C19 |
| MFID0939 | NM_000769.4:c.-889T>G | single nucleotide variant | CYP2C19 |
| MFID0940 | NM_000771.4:c.1075A>C | single nucleotide variant | CYP2C9 |
| MFID0941 | NM_000777.5:c.219-237A>G | single nucleotide variant | CYP3A5 |
| MFID0942 | NM_000789.4:c.2189C>A | single nucleotide variant | ACE |
| MFID0943 | NM_000789.4:c.2328G>A | single nucleotide variant | ACE |
| MFID0944 | NM_000789.4:c.2371C>T | single nucleotide variant | ACE |
| MFID0945 | NM_000789.4:c.-240A>T | single nucleotide variant | ACE |
| MFID0946 | NM_000789.4:c.3683C>T | single nucleotide variant | ACE |
| MFID0947 | NM_000792.7:c.*1058A>G | single nucleotide variant | DIO1 |
| MFID0948 | NM_000792.7:c.*29C>T | single nucleotide variant | DIO1 |
| MFID0949 | NM_000794.5:c.-48A>G | single nucleotide variant | DRD1 |
| MFID0950 | NM_000852.4:c.313A>G | single nucleotide variant | GSTP1 |
| MFID0951 | NM_000859.3:c.2458-84C>T | single nucleotide variant | HMGCR |
| MFID0952 | NM_000895.3:c.290+456A>G | single nucleotide variant | LTA4H |
| MFID0953 | NM_000895.3:c.88-6820C>T | single nucleotide variant | LTA4H |
| MFID0954 | NM_000906.4:1024G>C | single nucleotide variant | NPR1 |
| MFID0955 | NM_000927.5:c.3085-72C>T | single nucleotide variant | ABCB1 |
| MFID0956 | NM_000927.5:c.3435T>C | single nucleotide variant | ABCB1 |
| MFID0957 | NM_000930.5:c.-7351C>T | single nucleotide variant | PLAT |
| MFID0958 | NM_000961.4:c.1117C>A | single nucleotide variant | PTGIS |
| MFID0959 | NM_000962.4:c.-842A>G | single nucleotide variant | PTGS1 |
| MFID0960 | NM_000963.4c.-765G>C | single nucleotide variant | PTGS2 |
| MFID0961 | NM_001001547.3:c.158C>A | single nucleotide variant | CD36 |
| MFID0962 | NM_001006630.2:c.*295T>A | single nucleotide variant | CHRM2 |
| MFID0963 | NM_001061.7:c.1134+2566A>C | single nucleotide variant | TBXAS1 |
| MFID0964 | NM_001061.7:c.1135-21195C>T | single nucleotide variant | TBXAS1 |
| MFID0965 | NM_001061.7:c.539+1001C>T | single nucleotide variant | TBXAS1 |
| MFID0966 | NM_001065.4:c.362G>A | single nucleotide variant | TNFRSF1A |
| MFID0967 | NM_001080471.3:c.3108C>T | single nucleotide variant | PEAR1 |
| MFID0968 | NM_001083899.2:c.13254T>C | single nucleotide variant | GP6 |
| MFID0969 | NM_001109.5:c.*137T>G | single nucleotide variant | ADAM8 |
| MFID0970 | NM_001123396.4:c.190G>A | single nucleotide variant | CCR2 |
| MFID0971 | NM_001127891.3:c.-1306C>T | single nucleotide variant | MMP2 |
| MFID0972 | NM_001127891.3:c.-1575G>A | single nucleotide variant | MMP2 |
| MFID0973 | NM_001127891.3:c.-735C>T | single nucleotide variant | MMP2 |
| MFID0974 | NM_001128849.3:c.4521-5330G>T | single nucleotide variant | SMARCA4 |
| MFID0975 | NM_001136.5:c.1704C>T | single nucleotide variant | AGER |
| MFID0976 | NM_001136.5:c.-429T>C | single nucleotide variant | AGER |
| MFID0977 | NM_001144382.2:c.3205-6841A>G | single nucleotide variant | PLCL2 |
| MFID0978 | NM_001154.4:c.-1C>T | single nucleotide variant | ANXA5 |
| MFID0979 | NM_001161352.2:c.687C>T | single nucleotide variant | KCNMA1 |
| MFID0980 | NM_001178.6:c.1411+333A>G | single nucleotide variant | ARNTL |
| MFID0981 | NM_001178.6:c.460-1731A>G | single nucleotide variant | ARNTL |
| MFID0982 | NM_001242767.2:c.1260-4955G>A | single nucleotide variant | MTHFD1L |
| MFID0983 | NM_001266.5:c.224G>A | single nucleotide variant | CES1 |
| MFID0984 | NM_001272034.2:c.636G>T | single nucleotide variant | STXBP2 |
| MFID0985 | NM_001303007.2:c.-1151A>C | single nucleotide variant | DDAH2 |
| MFID0986 | NM_001308093.3:c.-333G>C | single nucleotide variant | GATA4 |
| MFID0987 | NM_001308093.3:c.-427C>T | single nucleotide variant | GATA4 |
| MFID0988 | NM_001308093.3:c.9C>T | single nucleotide variant | GATA4 |
| MFID0989 | NM_001318787.2:c.1350T>C | single nucleotide variant | TLR2 |
| MFID0990 | NM_001337.4:c.745G>A | single nucleotide variant | CX3CR1 |
| MFID0991 | NM_001337.4:c.839C>T | single nucleotide variant | CX3CR1 |
| MFID0992 | NM_001350001.2:c.2591G>C | single nucleotide variant | JCAD |
| MFID0993 | NM_001354761.2:c.1378G>T | single nucleotide variant | ADD1 |
| MFID0994 | NM_001371904.1:c.-1131T>C | single nucleotide variant | APOA5 |
| MFID0995 | NM_000384.3:c.10913G>A | single nucleotide variant | APOB |
| MFID0996 | NM_001371904.1:c.56C>G | single nucleotide variant | APOA5 |
| MFID0997 | NM_001384479.1:c.593C>T | single nucleotide variant | AGT |
| MFID0998 | NM_001384479.1:c.704T>C | single nucleotide variant | AGT |
| MFID0999 | NM_001386809.1:c.*A>C | single nucleotide variant | CXCL16 |
| MFID1000 | NM_001386809.1:c.368T>C | single nucleotide variant | CXCL16 |
| MFID1001 | NM_001394783.1:c.554_585del | single nucleotide variant | CCR5 |
| MFID1002 | NM_001408.3:c.*A>G | single nucleotide variant | CELSR2 |
| MFID1003 | NM_001437.3:c.*39G>A | single nucleotide variant | ESR2 |
| MFID1004 | NM_001437.3:c.-789T>G | single nucleotide variant | ESR2 |
| MFID1005 | NM_001437.3:c.984G>A | single nucleotide variant | ESR2 |
| MFID1006 | NM_001441.3:c.385C>A | single nucleotide variant | FAAH |
| MFID1007 | NM_001498.4:c.-129C>T | single nucleotide variant | GCLC |
| MFID1008 | NM_001559.3:c.1459+514A>C | single nucleotide variant | IL12RB2 |
| MFID1009 | NM_001562.4:c.*183A>G | single nucleotide variant | IL18 |
| MFID1010 | NM_001562.4:c.-105C>T | single nucleotide variant | IL18 |
| MFID1011 | NM_001562.4:c.361-221C>A | single nucleotide variant | IL18 |
| MFID1012 | NM_001562.4:c.-607C>T | single nucleotide variant | IL18 |
| MFID1013 | NM_001562.4:c.-656G>T | single nucleotide variant | IL18 |
| MFID1014 | NM_001562.4:c.-8-1360A>G | single nucleotide variant | IL18 |
| MFID1015 | NM_001562.4:c.-9+3005A>G | single nucleotide variant | IL18 |
| MFID1016 | NM_001562.4:c.91+488G>C | single nucleotide variant | IL18 |
| MFID1017 | NM_001622.4:c.743T>C | single nucleotide variant | AHSG |
| MFID1018 | NM_001622.4:c.767G>C | single nucleotide variant | AHSG |
| MFID1019 | NM_001753.5:c.196-12759A>G | single nucleotide variant | CAV1 |
| MFID1020 | NM_001845.6:c.4002A>C | single nucleotide variant | COL4A1 |
| MFID1021 | NM_001846.4:c.99+242A>G | single nucleotide variant | COL4A2 |
| MFID1022 | NM_001872.5:c.1040C>T | single nucleotide variant | CPB2 |
| MFID1023 | NM_001904.4:c.2340C>T | single nucleotide variant | CTNNB1 |
| MFID1024 | NM_001935.4:c.366+1153G>A | single nucleotide variant | DPP4 |
| MFID1025 | NM_001957.4:c.-231A>G | single nucleotide variant | EDNRA |
| MFID1026 | NM_001972.4:c.-761G>A | single nucleotide variant | ELANE |
| MFID1027 | NM_001992.5:c.-1738G>A | single nucleotide variant | F2R |
| MFID1028 | NM_001992.5:c.2860G>A | single nucleotide variant | F2R |
| MFID1029 | NM_001993.5:c.-603A>G | single nucleotide variant | F3 |
| MFID1030 | NM_001994.3:c.344G>A | single nucleotide variant | F13B |
| MFID1031 | NM_002000.4:c.337G>A | single nucleotide variant | FCAR |
| MFID1032 | NM_002060.3:c.955C>T | single nucleotide variant | GJA4 |
| MFID1033 | NM_002061.4:c.-588C>T | single nucleotide variant | GCLM |
| MFID1034 | NM_002075.4:c.825C>T | single nucleotide variant | GNB3 |
| MFID1035 | NM_002133.3:c.-413T>A | single nucleotide variant | HMOX1 |
| MFID1036 | NM_002182.4:c.1051+6959A>T | single nucleotide variant | IL1RAP |
| MFID1037 | NM_002184.4:c.442G>C | single nucleotide variant | IL6ST |
| MFID1038 | NM_002188.3:c.431A>G | single nucleotide variant | IL13 |
| MFID1039 | NM_002203.4:c.672T>C | single nucleotide variant | ITGA2 |
| MFID1040 | NM_002203.4:c.759C>T | single nucleotide variant | ITGA2 |
| MFID1041 | NM_002217.4:c.108G>A | single nucleotide variant | ITIH3 |
| MFID1042 | NM_002250.3:c.820-60G>A | single nucleotide variant | KCNN4 |
| MFID1043 | NM_002253.4:c.-604T>C | single nucleotide variant | KDR |
| MFID1044 | NM_002257.4:c.556A>G | single nucleotide variant | KLK1 |
| MFID1045 | NM_002303.6:c.326A>G | single nucleotide variant | LEPR |
| MFID1046 | NM_002303.6:c.668A>G | single nucleotide variant | LEPR |
| MFID1047 | NM_002421.4:c.-422A>T | single nucleotide variant | MMP1 |
| MFID1048 | NM_002421.4:c.-519A>G | single nucleotide variant | MMP1 |
| MFID1049 | NM_002422.5:c.-376C>G | single nucleotide variant | MMP3 |
| MFID1050 | NM_002543.4:c.*188C>T | single nucleotide variant | OLR1 |
| MFID1051 | NM_002543.4:c.501G>C | single nucleotide variant | OLR1 |
| MFID1052 | NM_002566.5:c.259G>A | single nucleotide variant | P2RY11 |
| MFID1053 | NM_002594.5:c.886-101G>C | single nucleotide variant | PCSK2 |
| MFID1054 | NM_002658.6:c.*141C>T | single nucleotide variant | PLAU |
| MFID1055 | NM_002791.3:c.-8C>G | single nucleotide variant | PSMA6 |
| MFID1056 | NM_002985.3:c.-403G>A | single nucleotide variant | CCL5 |
| MFID1057 | NM_002986.3:c.-2578G>A | single nucleotide variant | CCL2 |
| MFID1058 | NM_002986.3:c.67G>A | single nucleotide variant | CCL11 |
| MFID1059 | NM_003005.4:c.-1817T>C | single nucleotide variant | SELP |
| MFID1060 | NM_003005.4:c.2266A>C | single nucleotide variant | SELP |
| MFID1061 | NM_003005.4:c.625G>A | single nucleotide variant | SELP |
| MFID1062 | NM_003005.4:c.992G>A | single nucleotide variant | SELP |
| MFID1063 | NM_003102.4:c.691C>G | single nucleotide variant | SOD3 |
| MFID1064 | NM_003246.4:c.2099A>G | single nucleotide variant | THBS1 |
| MFID1065 | NM_003247.5:c.*191T>G | single nucleotide variant | THBS2 |
| MFID1066 | NM_003248.6:c.1159G>C | single nucleotide variant | THBS4 |
| MFID1067 | NM_003255.5:c.-4804T>G | single nucleotide variant | TIMP2 |
| MFID1068 | NM_003326.5:c.153+331T>C | single nucleotide variant | TNFSF4 |
| MFID1069 | NM_003326.5:c.154-5804T>C | single nucleotide variant | TNFSF4 |
| MFID1070 | NM_003355.3:c.-866G>A | single nucleotide variant | UCP2 |
| MFID1071 | NM_003376.6:c.-2578A>C | single nucleotide variant | VEGFA |
| MFID1072 | NM_003376.6:c.-460C>T | single nucleotide variant | VEGFA |
| MFID1073 | NM_003376.6:c.-94C>G | single nucleotide variant | VEGFA |
| MFID1074 | NM_003455.4:c.461C>T | single nucleotide variant | ZNF202 |
| MFID1075 | NM_003719.5:c.339+11353G>A | single nucleotide variant | PDE8B |
| MFID1076 | NM_003882.4:c.69+2823C>T | single nucleotide variant | CCN4 |
| MFID1077 | NM_003904.5:c.*724C>G | single nucleotide variant | ZPR1 |
| MFID1078 | NM_004064.5:c.-838C>A | single nucleotide variant | CDKN1B |
| MFID1079 | NM_004186.5:c.1947+46A>G | single nucleotide variant | SEMA3F |
| MFID1080 | NM_004599.4:c.1784G>C | single nucleotide variant | SREBF2 |
| MFID1081 | NM_004631.5:c.2855G>A | single nucleotide variant | LRP8 |
| MFID1082 | NM_004640.7:c.-23C>G | single nucleotide variant | DDX39B |
| MFID1083 | NM_004771.4:c.53A>C | single nucleotide variant | MMP20 |
| MFID1084 | NM_004797.4:c.-11377C>G | single nucleotide variant | ADIPOQ |
| MFID1085 | NM_004797.4:c.-11391G>A | single nucleotide variant | ADIPOQ |
| MFID1086 | NM_004797.4:c.214+62G>T | single nucleotide variant | ADIPOQ |
| MFID1087 | NM_004797.4:c.323C>T | single nucleotide variant | ADIPOQ |
| MFID1088 | NM_004797.4:c.45T>G | single nucleotide variant | ADIPOQ |
| MFID1089 | NM_004827.3:c.421C>A | single nucleotide variant | ABCG2 |
| MFID1090 | NM_004864.4:c.142T>A | single nucleotide variant | GDF15 |
| MFID1091 | NM_004864.4:c.-3148C>G | single nucleotide variant | GDF15 |
| MFID1092 | NM_004895.5:c.14229A>T | single nucleotide variant | NLRP3 |
| MFID1093 | NM_004895.5:c.14240C>T | single nucleotide variant | NLRP3 |
| MFID1094 | NM_004895.5:c.14261A>C | single nucleotide variant | NLRP3 |
| MFID1095 | NM_004895.5:c.14347A>G | single nucleotide variant | NLRP3 |
| MFID1096 | NM_004895.5:c.2113C>A | single nucleotide variant | NLRP3 |
| MFID1097 | NM_004898.4:c.1450-143A>G | single nucleotide variant | CLOCK |
| MFID1098 | NM_004898.4:c.793-1130T>C | single nucleotide variant | CLOCK |
| MFID1099 | NM_004936.4:c.*656A>C | single nucleotide variant | CDKN2B |
| MFID1100 | NM_004994.3:c.-1562C>T | single nucleotide variant | MMP9 |
| MFID1101 | NM_004994.3:c.836A>G | single nucleotide variant | MMP9 |
| MFID1102 | NM_005036.6:c.1047+2528C>G | single nucleotide variant | PPARA |
| MFID1103 | NM_005036.6:c.-127+2233A>G | single nucleotide variant | PPARA |
| MFID1104 | NM_005036.6:c.-127+5156G>A | single nucleotide variant | PPARA |
| MFID1105 | NM_005036.6:c.484C>G | single nucleotide variant | PPARA |
| MFID1106 | NM_005037.7:c.-689C>T | single nucleotide variant | PPARG |
| MFID1107 | NM_005084.4:c.1136T>C | single nucleotide variant | PLA2G7 |
| MFID1108 | NM_005084.4:c.28400C>G | single nucleotide variant | PLA2G7 |
| MFID1109 | NM_005084.4:c.835G>T | single nucleotide variant | PLA2G7 |
| MFID1110 | NM_005141.5:c.1433G>A | single nucleotide variant | FGB |
| MFID1111 | NM_005141.5:c.-148C>T | single nucleotide variant | FGB |
| MFID1112 | NM_005141.5:c.17382G>T | single nucleotide variant | FGB |
| MFID1113 | NM_005141.5:c.-249C>T | single nucleotide variant | FGB |
| MFID1114 | NM_005141.5:c.-455G>A | single nucleotide variant | FGB |
| MFID1115 | NM_005163.2:c.175+18C>T | single nucleotide variant | AKT1 |
| MFID1116 | NM_005214.5:c.49A>G | single nucleotide variant | CTLA4 |
| MFID1117 | NM_005215.4:c.92-120346C>T | single nucleotide variant | DCC |
| MFID1118 | NM_005223.4:c.731G>A | single nucleotide variant | DNASE1 |
| MFID1119 | NM_005502.4:c.2649A>G | single nucleotide variant | ABCA1 |
| MFID1120 | NM_005502.4:c.-565C>T | single nucleotide variant | ABCA1 |
| MFID1121 | NM_005502.4:c.656G>A | single nucleotide variant | ABCA1 |
| MFID1122 | NM_005505.5:c.1050T>C | single nucleotide variant | SCARB1 |
| MFID1123 | NM_005505.5:c.127-10172C>G | single nucleotide variant | SCARB1 |
| MFID1124 | NM_005544.3:c.2911G>A | single nucleotide variant | IRS1 |
| MFID1125 | NM_005577.4:c.5673A>G | single nucleotide variant | LPA |
| MFID1126 | NM_005956.4:c.-105C>T | single nucleotide variant | MTHFD1 |
| MFID1127 | NM_005956.4:c.1958G>A | single nucleotide variant | MTHFD1 |
| MFID1128 | NM_005957.5:c.1286A>C | single nucleotide variant | MTHFR |
| MFID1129 | NM_005957.5:c.665C>T | single nucleotide variant | MTHFR |
| MFID1130 | NM_005958.4:c.497G>A | single nucleotide variant | MTNR1A |
| MFID1131 | NM_005959.5:c.223+5596C>G | single nucleotide variant | MTNR1B |
| MFID1132 | NM_006033.4:c.332C>T | single nucleotide variant | LIPG |
| MFID1133 | NM_006172.4:c.454T>C | single nucleotide variant | NPPA |
| MFID1134 | NM_006208.3:c.517A>C | single nucleotide variant | ENPP1 |
| MFID1135 | NM_006440.5:c.50964T>C | single nucleotide variant | TXNRD2 |
| MFID1136 | NM_006498.3:c.6+3279C>T | single nucleotide variant | LGALS2 |
| MFID1137 | NM_006768.5:c.443+270A>G | single nucleotide variant | BRAP |
| MFID1138 | NM_006768.5:c.723A>G | single nucleotide variant | BRAP |
| MFID1139 | NM_007202.4:c.1936A>G | single nucleotide variant | AKAP10 |
| MFID1140 | NM_012238.5:c.943-3428C>G | single nucleotide variant | SIRT1 |
| MFID1141 | NM_013989.5:c.*1453C>T | single nucleotide variant | DIO2 |
| MFID1142 | NM_013989.5:c.274A>G | single nucleotide variant | DIO2 |
| MFID1143 | NM_014272.5:c.640T>C | single nucleotide variant | ADAMTS7 |
| MFID1144 | NM_014479.3:c.1331A>G | single nucleotide variant | ADAMDEC1 |
| MFID1145 | NM_015869.5:c.34C>G | single nucleotide variant | PPARG |
| MFID1146 | NM_016179.4:c.2869A>G | single nucleotide variant | TRPC4 |
| MFID1147 | NM_016179.4:c.898-13958T>C | single nucleotide variant | TRPC4 |
| MFID1148 | NM_016215.5:c.572-117C>T | single nucleotide variant | MIR126 |
| MFID1149 | NM_016818.3:c.1889C>T | single nucleotide variant | ABCG1 |
| MFID1150 | NM_016818.3:c.-311T>A | single nucleotide variant | ABCG1 |
| MFID1151 | NM_016818.3:c.-376C>T | single nucleotide variant | ABCG1 |
| MFID1152 | NM_017435.5:c.1383-99A>G | single nucleotide variant | SLCO1C1 |
| MFID1153 | NM_017435.5:c.271+1368T>C | single nucleotide variant | SLCO1C1 |
| MFID1154 | NM_017435.5:c.405-747A>G | single nucleotide variant | SLCO1C1 |
| MFID1155 | NM_017649.5:c.1621+39238G>A | single nucleotide variant | CNNM2 |
| MFID1156 | NM_019616.4:c.1172G>A | single nucleotide variant | F7 |
| MFID1157 | NM_019616.4:c.-402G>A | single nucleotide variant | F7 |
| MFID1158 | NM_019616.4:c.64+9G>A | single nucleotide variant | F7 |
| MFID1159 | NM_020297.5:c.2200G>A | single nucleotide variant | ABCC9 |
| MFID1160 | NM_021995.2:c.266G>A | single nucleotide variant | UTS2 |
| MFID1161 | NM_022788.5:c.36T>G | single nucleotide variant | P2RY12 |
| MFID1162 | NM_022817.3:c.3731G>A | single nucleotide variant | PER2 |
| MFID1163 | NM_024006.6:c.*134G>A | single nucleotide variant | VKORC1 |
| MFID1164 | NM_024420.3:c.115+9538A>G | single nucleotide variant | PLA2G4A |
| MFID1165 | NM_024551.3:c.-86-6442T>C | single nucleotide variant | ADIPOR2 |
| MFID1166 | NM_025144.4:c.2608G>A | single nucleotide variant | ALPK1 |
| MFID1167 | NM_025144.4:c.2746A>G | single nucleotide variant | ALPK1 |
| MFID1168 | NM_030948.6:c.250+151419C>A | single nucleotide variant | PHACTR1 |
| MFID1169 | NM_030948.6:c.251-126053C>G | single nucleotide variant | PHACTR1 |
| MFID1170 | NM_032951.3:c.723G>C | single nucleotide variant | MLXIPL |
| MFID1171 | NM_052890.4:c.809T>A | single nucleotide variant | PGLYRP2 |
| MFID1172 | NM_080429.3:c.367C>T | single nucleotide variant | AQP10 |
| MFID1173 | NM_080748.3:c.132-494T>C | single nucleotide variant | ROMO1 |
| MFID1174 | NM_138554.5:c.896A>G | single nucleotide variant | TLR4 |
| MFID1175 | NM_138711.6:c.1341C>T | single nucleotide variant | PPARG |
| MFID1176 | NM_145027.6:c.2155T>C | single nucleotide variant | KIF6 |
| MFID1177 | NM_153756.3:c.499+250C>T | single nucleotide variant | FNDC5 |
| MFID1178 | NM_174936.4:c.137G>A | single nucleotide variant | PCSK9 |
| MFID1179 | NM_174936.4:c.94G>A | single nucleotide variant | PCSK9 |
| MFID1180 | NM_182632.3:c.957C>G | single nucleotide variant | SLC6A18 |
| MFID1181 | NM_182751.3:c.1621A>T | single nucleotide variant | MCM10 |
| MFID1182 | NM_182982.3:c.1457T>C | single nucleotide variant | GRK4 |
| MFID1183 | NM_198056.3:c.-52-562G>C | single nucleotide variant | SCN5A |
| MFID1184 | NM_198129.4:c.3720-325G>A | single nucleotide variant | LAMA3 |
| MFID1185 | NM_198551.4:c.3632-105A>C | single nucleotide variant | MIA3 |
| MFID1186 | NM_199168.4:c.801G>A | single nucleotide variant | CXCL12 |
| MFID1187 | NP_000518.1:p. | single nucleotide variant | LDLR |
| MFID1188 | NP_000952.1:p.Glu461Ala | single nucleotide variant | PTGIS |
| MFID1189 | NP_001052.3:p.Pro1770Leu | single nucleotide variant | TBXAS1 |
| MFID1190 | NR_002819.4:n.6624C>T | single nucleotide variant | MALAT1 |
| MFID1191 | NR_003491.3:c.11093G>A | single nucleotide variant | MIAT |
| MFID1192 | NR_003491.3:c.11741G>A | single nucleotide variant | MIAT |
| MFID1193 | NR_003491.3:c.12311C>T | single nucleotide variant | MIAT |
| MFID1194 | NR_003491.3:c.8813G>A | single nucleotide variant | MIAT |
| MFID1195 | NR_003491.3:n.1505G>A | single nucleotide variant | MIAT |
| MFID1196 | NR_003529.3:n.1155C>G | single nucleotide variant | CDKN2B-AS1 |
| MFID1197 | NR_003529.3:n.385G>A | single nucleotide variant | CDKN2B-AS1 |
| MFID1198 | NR_003529.3:n.487T>C | single nucleotide variant | CDKN2B-AS1 |
| MFID1199 | NR_029501.1:n.40A>G | single nucleotide variant | MIR27A |
| MFID1200 | NR_029617.1:n.78C>T | single nucleotide variant | MIR196A2 |
| MFID1201 | NR_030223.1:n.73A>G | single nucleotide variant | MIR499A |
| MFID1202 | NR_038911.1:n.17G>A | single nucleotide variant | MIF |
| MFID1203 | NM_000761.5:c.-2964G>A | single nucleotide variant | CYP1A2 |
| MFID1204 | NM_002427.4:c.799+92A>G | single nucleotide variant | MMP13 |
| MFID1205 | NM_147686.4:c.-9+4259T>C | single nucleotide variant | TRAF3IP2 |
| MFID1206 | NM_003255.5:c.-2803T>C | single nucleotide variant | TIMP2 |
| MFID1207 | m.16356T>C | single nucleotide variant | None |
| MFID1208 | m.72T>C | single nucleotide variant | None |
| MFID1209 | m.73A>G | single nucleotide variant | None |
| MFID1210 | NM_001136.5:c.-374T>A | single nucleotide variant | AGER |
| MFID1211 | NG_051108.1:g.68130T>C | single nucleotide variant | HHIPL1 |
| MFID1212 | NM_001005487.2:c.394A>G | single nucleotide variant | OR13G1 |
| MFID1213 | NM_001166108.2:c.1964+44318A>G | single nucleotide variant | PALLD |
| MFID1214 | NM_002581.5:c.2233+95G>C | single nucleotide variant | PAPPA |
| MFID1215 | NM_000602.5:c.-844G>A | single nucleotide variant | SERPINE1 |
| MFID1216 | NG_007373.1:g.4100A>G | single nucleotide variant | TBX5 |
| MFID1217 | NG_007373.1:g.4194G>A | single nucleotide variant | TBX5 |
| MFID1218 | NG_007373.1:g.4260T>C | single nucleotide variant | TBX5 |
| MFID1219 | NG_007373.1:g.4367C>A | single nucleotide variant | TBX5 |
| MFID1220 | NG_007373.1:g.4581A>G | single nucleotide variant | TBX5 |
| MFID1221 | NG_007373.1:g.5004G>T | single nucleotide variant | TBX5 |
| MFID1826 | NM_002564.4:c.*6158G>A | single nucleotide variant | P2RY2 |