A total of 530 results found based on your keywords
RF_ID Disease Name poly_category variablesites Species RF_Name Association Condition PMID
3826 Parkinson disease SNP TMEM163 p.33P>R Human TMEM RF 33279243
3825 Parkinson disease SNP TMEM175 p.176 K>E Human TMEM RF 33279243
4008 Fatal familial insomnia (FFI) SNP rs169172 Human SRSF11 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4007 Fatal familial insomnia (FFI) SNP rs647872 Human SRSF11 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4009 Fatal familial insomnia (FFI) SNP rs10661326 Human SRSF11 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4000 Fatal familial insomnia (FFI) SNP rs360609 Human NR1H9P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
3999 Fatal familial insomnia (FFI) SNP rs75631798 Human NR1H8P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
3998 Fatal familial insomnia (FFI) SNP rs360608 Human NR1H7P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
3997 Fatal familial insomnia (FFI) SNP rs360607 Human NR1H6P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
3996 Fatal familial insomnia (FFI) SNP rs360599 Human NR1H5P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4001 Fatal familial insomnia (FFI) SNP rs360610 Human NR1H10P RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4011 Fatal familial insomnia (FFI) SNP rs60353063 Human MSANTD3 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4013 Fatal familial insomnia (FFI) SNP rs73655549 Human MSANTD3 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4010 Fatal familial insomnia (FFI) SNP rs57241635 Human MSANTD3 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4012 Fatal familial insomnia (FFI) SNP rs10114432 Human MSANTD3 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4014 Fatal familial insomnia (FFI) SNP rs1556487 Human MSANTD3 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4003 Fatal familial insomnia (FFI) SNP rs2685151 Human GNA13P1 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4002 Fatal familial insomnia (FFI) SNP rs1594400 Human GNA13P1 RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4005 Fatal familial insomnia (FFI) SNP rs1992813 Human EXOC1L RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4004 Fatal familial insomnia (FFI) SNP rs1447039 Human EXOC1L RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
4006 Fatal familial insomnia (FFI) SNP rs1447049 Human EXOC1L RF These genetic variants are absent in FFI patients with early disease onset (19-40 years) 37626863
1839 Alzheimer's Disease SNP rs41453547 A5656G Human MT-ND2 RF 34854014
1840 Alzheimer's Disease SNP rs386420024 A13759G Human MT-ND5 RF 34854014
3990 Tourette Syndrome SNP rs35615695 Human ASH1L RF 35307981
3989 Tourette Syndrome SNP rs5005770 Human ASH1L RF 35307981
470 Multiple System Atrophy SNP rs11931074 (GG) Human SNCA + well water nondrinkers PF 35748722
467 Multiple System Atrophy SNP rs11931074 (tt) Human SNCA + alcohol nonusers PF 35748722
468 Multiple System Atrophy SNP rs148156462 (TT) Human COQ2 + current smokers PF 35748722
466 Multiple System Atrophy SNP rs148156462 (Tc) Human COQ2 + pesticide nonexposure PF 35748722
1666 Amyotrophic Lateral Sclerosis SNP 12q13.3(rs60565245) Human LRP1 RF 37142397
1571 Amyotrophic Lateral Sclerosis SNP 7p21.3(rs2354952) Human THSD7A RF 37142397
1677 Amyotrophic Lateral Sclerosis SNP 5q31.3(rs11738209) Human FGF1 RF 37142397
1829 Parkinson disease SNP rs3746106 5'-UTR Human MIDN RF 36858566
3952 Parkinson disease SNP rs1922452/A allelic variant Human CD4 RF 36224715
3953 Parkinson disease SNP rs951818/A Human CD4 RF 36224715
3930 Alzheimer's Disease SNP rs2421943 GG and AG genotypes Human IDE RF 35236268
3904 Alzheimer's Disease SNP minor allele of rs5025718 Human NOTCH2 RF 37355909
3147 Amyotrophic Lateral Sclerosis SNP Human A90V TDP-43 variant RF 18505686
721 Alzheimer's Disease SNP rs3752246 Human ABCA7 PF National Alzheimer’s Coordinating Center (NACC) cohort 30128317
1942 Alzheimer's Disease SNP rs3764650 G allele Human ABCA7 RF 26795201
1974 Alzheimer's Disease SNP rs3764650 Human ABCA7 RF Calculated by fixed effect model 29504051
767 Parkinson disease SNP TCG (rs3764650-rs3752246-rs4147929) haplotype Human ABCA7 PF 35709878
2972 Alzheimer's Disease SNP rs3764650 Human ABCA7 RF 29589097
3955 Parkinson disease SNP A allele of rs4147929 Human ABCA7 RF 35709878
3149 Alzheimer's Disease SNP rs142076058 Human ABCA7 RF 29589097
3110 Parkinson disease SNP g.116154T>C (rs28746504), g.117130A>G (rs2188524), g.117356C>G (rs34976462), g.117372T>C (rs3213619) Human ABCB1 RF 24572589
546 Alzheimer's Disease SNP rs2247071、rs2862616、rs3753526、rs1044925:CGCA Haplotype Human ACAT1 PF 33057949
2349 Alzheimer's Disease SNP rs2247071、rs2862616、rs3753526、rs1044925:CGGA Haplotype Human ACAT1 RF 33057949
3152 Alzheimer's Disease SNP rs4343 Human ACE RF in subjects aged 73 years and above. 19539712
3835 Parkinson disease SNP rs4646994 polymorphisms Human ACE RF 34945793
3151 Alzheimer's Disease SNP rs4293 Human ACE RF 21537449
3153 Alzheimer's Disease SNP rs1799752 Human ACE RF in subjects aged 73 years and above. 19539712
2513 Parkinson disease SNP rs1229984T allele Human ADH1B RF 30483881
3155 Alzheimer's Disease SNP rs4769874 A-allele and AA genotype Human ALOX5 RF 26944113
2325 Alzheimer's Disease SNP rs515071 polymorphism Human ANK1 RF 26611832
3856 Parkinson disease SNP rs2734849 GG homozygotes Human ANKK1 RF 34151861
3156 Alzheimer's Disease SNP rs4420638 polymorphisms Human APOC1 RF 30443289
1656 Alzheimer's Disease SNP rs12721046 Human APOC1 RF using Cox regression、Dataset：FHS（Framingham Heart Study） 29107063
1670 Alzheimer's Disease SNP rs12721046 Human APOC1 RF using Cox regression、Dataset：CHS（Cardiovascular Health Study） 29107063
3157 Alzheimer's Disease SNP rs11568822 polymorphism Human APOC1 RF not in African Americans 24498013
2536 Alzheimer's Disease SNP rs12721046 Human APOC1 RF using logistic regression、Dataset：FHS(Framingham Heart Study) 29107063
3695 Alzheimer's Disease SNP rs429358 Human APOE RF 34336000
2976 Alzheimer's Disease SNP rs429358, rs7412 Human APOE RF ε4 allele; AD without depression 29703883
2894 Alzheimer's Disease SNP rs429358, rs7412 Human APOE RF ε4 allele; AD all 29703883
3014 Alzheimer's Disease SNP rs429358, rs7412 Human APOE RF Genotype: ?3/?4; AD without depression 29703883
2774 Alzheimer's Disease SNP rs429358, rs7412 Human APOE RF Genotype: ?4/?4; AD without depression 29703883
2601 Alzheimer's Disease SNP rs449647 Human APOE RF A/A genotype 19172988
2897 Alzheimer's Disease SNP rs429358, rs7412 Human APOE RF Genotype: ?3/?4; AD all 29703883
1572 Alzheimer's Disease SNP rs405509 Human APOE RF using Cox regression、Dataset：CHS（Cardiovascular Health Study） 29107063
625 Alzheimer's Disease SNP rs449647 Human APOE PF Genotype/Allele: A/T 29990559
2087 Alzheimer's Disease SNP rs449647 Human APOE RF Genotype/Allele: A 29990559
3115 Alzheimer's Disease SNP rs429358 TC genotype Human APOE RF 35135450
719 Alzheimer's Disease SNP rs449647 Human APOE PF Genotype/Allele: T 29990559
2734 Alzheimer's Disease SNP L28P; rs769452 Human APOE RF with APOE*4?allele 36528961
2463 Alzheimer's Disease SNP rs429358 TT genotype Human APOE RF 35135450
2298 Alzheimer's Disease SNP rs449647 Human APOE RF Genotype/Allele: A/A 29990559
2912 Alzheimer's Disease SNP rs7412 TT genotype Human APOE RF 35135450
2610 Dementia with Lewy bodies SNP rs429358 Human APOE RF 29263008
2260 Alzheimer's Disease SNP rs405509 Human APOE RF using logistic regression、Dataset：LOADFS(Late Onset Alzheimer's Disease Family Study ) 29107063
2368 Alzheimer's Disease SNP rs769449 Human APOE RF using logistic regression、Dataset：HRS(Health and Retirement Study) 29107063
1620 Alzheimer's Disease SNP rs769449 Human APOE RF using Cox regression、Dataset：HRS（Health and Retirement Study） 29107063
2113 Alzheimer's Disease SNP rs405509 Human APOE RF using logistic regression、Dataset：CHS( Cardiovascular Health Study) 29107063
2642 Lewy Body Disease SNP rs429358 Human APOE?4 RF 34308904
3914 Alzheimer's Disease SNP NM_000484.3: c.2045A > T; p.E682V Human APP RF 37145212
1800 Alzheimer's Disease SNP rs1801278 Human Arg972 IRS1 RF A Allele 24589556
1819 Alzheimer's Disease SNP rs1801278 Human Arg972 IRS1 RF AA genotype 24589556
1808 Alzheimer's Disease SNP rs1801278 Human Arg972 IRS1 RF GA genotype 24589556
3196 Alzheimer's Disease SNP rs16933774 Human ASTN2 RF 25410587
2580 Alzheimer's Disease SNP rs732774 Human ATP10B RF 22950421
2142 Alzheimer's Disease SNP rs1801243 Human ATP7B RF 22950421
2177 Alzheimer's Disease SNP rs2147363 Human ATP8B RF 22950421
2284 Alzheimer's Disease SNP rs1061472 Human ATP9B RF 22950421
3198 Amyotrophic Lateral Sclerosis SNP rs179943 Human ATXN1 RF 25023141
2413 Alzheimer's Disease SNP rs638405，Val262 CC genotype Human BACE1 RF in carrying the ApoE epsilon4 allele 18182766
1935 Alzheimer's Disease SNP rs2837960 G allele Human BACE2 RF Rheumatoid arthritis (RA) RA-SNPs Association with AD 21595938
3833 Parkinson disease SNP rs6265 polymorphisms Human BDNF RF 34945793
2353 Alzheimer's Disease SNP rs2030324 Human BDNF C270T RF 26136901
3205 Alzheimer's Disease SNP rs744373 polymorphism Human BIN1 RF 26768592
1920 Alzheimer's Disease SNP rs744373 Human BIN1 RF Calculated by fixed effect model 29504051
714 Alzheimer's Disease SNP rs7561528 Human BIN1 PF National Alzheimer’s Coordinating Center (NACC) cohort 30128317
1891 Alzheimer's Disease SNP rs744373 Human BIN1 RF Calculated by fixed effect model 29504051
1910 Alzheimer's Disease SNP rs744373 Human BIN1 RF Calculated by fixed effect model 29504051
3204 Alzheimer's Disease SNP rs12989701 polymorphism Human BIN1 RF 26768592
682 Alzheimer's Disease SNP rs6733839 Human BIN1 PF National Alzheimer’s Coordinating Center (NACC) cohort 30128317
1916 Alzheimer's Disease SNP rs744373 Human BIN1 RF Calculated by random effect model 29504051
1906 Alzheimer's Disease SNP rs744373 Human BIN1 RF Calculated by random effect model 29504051
2860 Frontotemporal Lobar Degeneration SNP rs61707463 Human C4orf27 RF Discovery stage 30739198
3206 Amyotrophic Lateral Sclerosis SNP rs2708851 Human C7orf57 RF 25023141
3207 Amyotrophic Lateral Sclerosis SNP rs3849942 Human C9orf72 RF 25023141
3051 Parkinson disease SNP Intermediate repeat copies Human C9orf72 RF 23845100
2409 Amyotrophic Lateral Sclerosis SNP rs774359 Human C9orf72 RF 20801718
729 Creutzfeldt-Jakob disease SNP rs4918016 Human CALHM1 PF 22874670
2544 Creutzfeldt-Jakob disease SNP rs41287502 Human CALHM1 RF Genotype:GG 22874670
1954 Alzheimer's Disease SNP P86L polymorphism (rs2986017) Human CALHM1 RF 20061624
3210 Parkinson disease SNP rs12817488 polymorphism Human CCDC62/HIP1R RF 25818163
1863 Parkinson disease SNP GRCh38.p12chr17：34252593 G> C Human CCL2 RF 30761072
1854 Parkinson disease SNP rs1024611 variants (T>C) Human CCL2 RF 30761072
926 Parkinson disease SNP GA genotype, rs3826656 Human CD33 PF 37479176
3954 Parkinson disease SNP A allele, rs12985029 Human CD33 RF 37479176
2162 Alzheimer's Disease SNP rs2455069-A>G (R69G) Human CD33 RF 35408990
815 Alzheimer's Disease SNP rs3865444 A allele Human CD33 PF this association was not significant in Asians 26795201
563 Alzheimer's Disease SNP rs3826656 AA genotype Human CD33 PF in APOE e4 carriers 22167654
901 Parkinson disease SNP rs3865444 Human CD33 PF 33582190
3213 Alzheimer's Disease SNP rs3865444 T allele Human CD33 RF 22382309
593 Alzheimer's Disease SNP rs3826656 A allele Human CD33 PF in APOE e4 carriers 22167654
3664 Alzheimer's Disease SNP rs2455069-A> G Human CD33 RF 32647856
2221 Alzheimer's Disease SNP rs7755 Human CD36 RF Genotype: Recessive 30235742
2477 Alzheimer's Disease SNP rs7755 Human CD36 RF Genotype: GG; Adjusting the physiological and biochemical factors, including age, FBG, BMI, SBP, DBP, HDLC [According to univariate analysis, there was a significant deviation (P<0.05)]. 30235742
2389 Alzheimer's Disease SNP rs7755 Human CD36 RF Genotype: Dominant 30235742
641 Alzheimer's Disease SNP rs3211956 Human CD36 PF Genotype: GT 30235742
630 Alzheimer's Disease SNP rs3211956 Human CD36 PF Genotype: GT; Adjusting the physiological and biochemical factors, including age, FBG, BMI, SBP, DBP, HDLC [According to univariate analysis, there was a significant deviation (P<0.05)]. 30235742
2598 Alzheimer's Disease SNP rs7755 Human CD36 RF Genotype: GG 30235742
2247 Alzheimer's Disease SNP rs7755 Human CD36 RF Genotype: Dominant; Adjusting the physiological and biochemical factors, including age, FBG, BMI, SBP, DBP, HDLC [According to univariate analysis, there was a significant deviation (P<0.05)]. 30235742
664 Alzheimer's Disease SNP rs3211956 Human CD36 PF Genotype: Dominant; Adjusting the physiological and biochemical factors, including age, FBG, BMI, SBP, DBP, HDLC [According to univariate analysis, there was a significant deviation (P<0.05)]. 30235742
681 Alzheimer's Disease SNP rs3211956 Human CD36 PF Genotype: Dominant 30235742
2203 Alzheimer's Disease SNP rs2177369 (G>A) Human CHAT RF 27272392
2236 Alzheimer's Disease SNP rs3810950 (G>A) Human CHAT RF 27272392
2878 Amyotrophic Lateral Sclerosis SNP P413L Human CHGB RF 20007371
2608 Amyotrophic Lateral Sclerosis SNP P413L Human CHGB RF 20007371
680 Alzheimer's Disease SNP rs4950928 Human CHI3L1 PF CG+GG 30223258
2551 Alzheimer's Disease SNP rs10399931 Human CHI3L1 RF TT 30223258
2127 Alzheimer's Disease SNP rs10399931 Human CHI3L1 RF T allele 30223258
687 Alzheimer's Disease SNP rs4950928 Human CHI3L1 PF G allele 30223258
2200 Alzheimer's Disease SNP rs10399931 Human CHI3L1 RF CT+TT 30223258
2595 Creutzfeldt-Jakob disease SNP Human CHN2 RF 22210626
3217 Alzheimer's Disease SNP rs7294919 polymorphism Human chromosome 12q24.22 RF 24361131
1991 Alzheimer's Disease SNP rs1333049 Human chromosome 9p21.3 RF C allele 19664850
2096 Alzheimer's Disease SNP rs1333049 C allele Human chromosome 9p21.3 RF in non-APOE epsilon4 20427016
2336 Alzheimer's Disease SNP rs1333049 polymorphism Human chromosome 9p21.3 RF 20427016
502 Alzheimer's Disease SNP rs9331888 GG+GC haplotypes Human CLU PF 26757186
1858 Alzheimer's Disease SNP rs11136000 Human CLU RF Calculated by fixed effect model 29504051
1860 Alzheimer's Disease SNP rs11136000 Human CLU RF Calculated by fixed effect model 29504051
2922 Alzheimer's Disease SNP rs1532278 GA genotype Human CLU RF 35135450
1859 Alzheimer's Disease SNP rs11136000 Human CLU RF Calculated by fixed effect model 29504051
1856 Alzheimer's Disease SNP rs11136000 Human CLU RF Calculated by random effect model 29504051
2969 Alzheimer's Disease SNP rs2279590 AA+GA haplotypes Human CLU RF 26757186
2072 Parkinson disease SNP rs9331896 TT genotype Human Clusterin (CLU) RF 33295114
2377 Tourette Syndrome SNP C allele of the rs2023239 Human CNR 1 RF 32194619
2134 Dementia with Lewy bodies SNP rs7314908 Human CNTN1 RF 29263008
2097 Amyotrophic Lateral Sclerosis SNP rs2619566 C Allele Human CNTN4 RF 34421992
465 Multiple System Atrophy SNP rs148156462 (TT) Human COQ2 PF 35748722
1899 Alzheimer's Disease SNP rs6656401 Human CR1 RF Calculated by fixed effect model 29504051
747 Alzheimer's Disease SNP rs6656401 Human CR1 PF National Alzheimer’s Coordinating Center (NACC) cohort 30128317
1905 Alzheimer's Disease SNP rs6656401 Human CR1 RF Calculated by fixed effect model 29504051
633 Alzheimer's Disease SNP rs6656401 Human CR1 PF PENN cohort 30128317
1979 Alzheimer's Disease SNP rs6656401 Human CR1 RF Calculated by fixed effect model 29504051
3122 Creutzfeldt-Jakob disease SNP rs17571 Human CTSD RF Genotype:CT 18426579
2632 Alzheimer's Disease SNP position 224 T-carrying genotype Human CTSD RF 24281128
2424 Creutzfeldt-Jakob disease SNP rs17571 Human CTSD RF Genotype:CC 18426579
2651 Amyotrophic Lateral Sclerosis SNP rs3732379 Human CX3CR1 RF 24806473
2362 Amyotrophic Lateral Sclerosis SNP rs3732379 Human CX3CR1 RF 24806473
3230 Amyotrophic Lateral Sclerosis SNP rs3732378 Human CX3CR1 RF 24806473
3232 Alzheimer's Disease SNP rs3751592 A/G polymorphism Human CYP19A1 RF 27583919
2710 Alzheimer's Disease SNP rs890293 Human CYP2J2 RF total;Genotype GT + TT 25796175
2687 Alzheimer's Disease SNP rs890293 Human CYP2J2 RF total;Allele T 25796175
2259 Alzheimer's Disease SNP rs754203 T allele Human CYP46A1 RF 22528464
3790 Amyotrophic lateral sclerosis,Parkinson disease SNP minor alleles of rs17115303 Human DAB1 RF 34707478
753 Alzheimer's Disease SNP C allele of rs4878104 Human DAPK1 PF especially the homozygotes 21167819
3832 Parkinson disease SNP rs2097629, rs1611115 polymorphisms Human DBH RF 34945793
2920 Frontotemporal Lobar Degeneration SNP rs4859146 Human DCUN1D1 RF Genotype:GG 19473369
1783 Alzheimer's Disease SNP rs12785878 T>C Human DHCR7 RF Chinese population 33692822
3235 Amyotrophic Lateral Sclerosis SNP rs16856202 Human DISC1 RF 25023141
2128 Parkinson disease SNP rs80315856 T allele Human DMRT2/SMARCA2 RF 33510632
3236 Parkinson disease SNP TT genotype and T allele of the 1254T>C polymorphism Human DMT1 RF 25817364
892 Parkinson disease SNP rs1451375 Polymorphisms Human DOPA decarboxylase gene (DDC) PF 33051953
3237 Amyotrophic Lateral Sclerosis SNP rs10260404 Human DPP6 RF 25023141
2627 Frontotemporal Lobar Degeneration SNP rs118113626 Human DPP6 RF Discovery stage 30739198
693 Amyotrophic Lateral Sclerosis SNP rs10260404 C Allele Human DPP6 PF 34421992
2621 Frontotemporal Lobar Degeneration SNP rs4726389 Human DPP6 RF Discovery stage 30739198
2765 Amyotrophic Lateral Sclerosis SNP rs147541241 Human DPYSL3(CRMP4) RF 23568759
648 Alzheimer's Disease SNP rs6557634;rs20575;rs20576 Human DR4 PF GGA haplotype 25207117
830 Alzheimer's Disease SNP rs6557634 Human DR4 PF the GA genotype 25207117
2076 Alzheimer's Disease SNP rs6557634;rs20575;rs20576 Human DR4 RF GCA haplotype 25207117
504 Alzheimer's Disease SNP rs6557634;rs20575;rs20576 Human DR4 PF GGC haplotype 25207117
581 Alzheimer's Disease SNP rs6557634;rs20575;rs20576 Human DR4 PF ACA haplotype 25207117
2384 Alzheimer's Disease SNP rs6557634;rs20575;rs20576 Human DR4 RF GCC haplotype 25207117
3834 Parkinson disease SNP rs6275, rs12364283, rs1076560 polymorphisms Human DRD2 RF 34945793
779 Progressive Supranuclear Palsy SNP rs6687758 Human DUSP10 PF Meta-analysis 29986742
2278 Parkinson disease SNP TT genotype derived from SNP rs8126696 Human DYRK1A RF especially for males 27546826
2038 Progressive Supranuclear Palsy SNP rs7571971 Human EIF2AK3 RF 33897612
765 Progressive Supranuclear Palsy SNP rs7571971 Human EIF2AK3 PF Meta-analysis 29986742
2222 Alzheimer's Disease SNP rs17247535 Human ENST00000414107 RF 29027019
3240 Amyotrophic Lateral Sclerosis SNP rs200746018 Human ERp57/PDIA3 RF 25913742
653 Alzheimer's Disease SNP rs3844508 Human ESR1 PF 20674091
2372 Alzheimer's Disease SNP rs10144225 G allele Human ESR2 RF predominantly Caucasian AIMS-defined ancestry 24326520
2194 Alzheimer's Disease SNP rs944045 G allele Human ESR2 RF predominantly Caucasian AIMS-defined ancestry 24326520
2371 Alzheimer's Disease SNP rs1256062 G allele Human ESR2 RF predominantly Caucasian AIMS-defined ancestry 24326520
2195 Alzheimer's Disease SNP rs2274705 G allele Human ESR2 RF predominantly Caucasian AIMS-defined ancestry 24326520
678 Alzheimer's Disease SNP rs10137185 T allele Human ESR3 PF 24326520
1925 Alzheimer's Disease SNP rs597668 C allele Human EXOC3L2 RF 28423615
814 Alzheimer's Disease SNP rs597668 C allele Human EXOC3L2 PF 28423615
703 Alzheimer's Disease SNP rs920608 C/A Allele Human FAM47E PF 33654092
3242 Parkinson disease SNP rs1721100 (C/G) polymorphism Human FGF20 RF 22342445
1911 Parkinson disease SNP rs1721100 GG genotype Human FGF20 RF 24942208
3140 Parkinson disease SNP rs12720208 polymorphism Human FGF20 RF 26070653
3241 Parkinson disease SNP rs12720208 polymorphism Human FGF20 RF 26070653
3244 Parkinson disease SNP rs1989754, ss20399075 Human FGF20 RF 15122513
2246 Alzheimer's Disease SNP rs7081208, rs2446581, rs17314229 AAC haplotype Human FRMD4A RF 22430674
785 Alzheimer's Disease SNP rs4945261 (G>A) Human GAB2 PF 26770425
2032 Alzheimer's Disease SNP C allele of the rs10793294 polymorphism Human GAB2 RF 21108942
2471 Alzheimer's Disease SNP C allele of rs7101429 Human GAB2 RF 21285854
3247 Alzheimer's Disease SNP T allele of rs4945261 Human GAB2 RF 21285854
3127 Alzheimer's Disease SNP rs2373115 polymorphism Human GAB2 RF a minor genetic determinant of AD 18272374
792 Alzheimer's Disease SNP rs2373115 (G>T) Human GAB2 PF 26770425
3248 Alzheimer's Disease SNP G allele of rs7115850 Human GAB2 RF 21285854
1923 Creutzfeldt-Jakob disease SNP rs2267161 Human GAL3ST1 RF 32949544
2647 Dementia with Lewy bodies SNP rs35749011 Human GBA RF 29263008
1838 Parkinson disease SNP rs3115534-G Human GBA1 RF 37633302
2179 Parkinson disease SNP rs3115534-G Human GBA1 RF 37633302
2293 Alzheimer's Disease SNP rs72713460 Human GCH1 RF 29432188
3260 Parkinson disease SNP RS11158026(T allele) polymorphism Human GCH1 RF 27871051
1989 Parkinson disease SNP Allele 'A' of rs797906 SNP Human GLIS1 RF 22759478
2065 Alzheimer's Disease SNP rs10868366 G allele Human GOLPH2 RF 22167654
2066 Alzheimer's Disease SNP rs7019241 C allele Human GOLPH2 RF 22167654
3261 Parkinson disease SNP rs4998386 T allele Human GRIN2A RF taking creatine who also have high levels of caffeine intake 28320167
1489 Frontotemporal Dementia SNP rs1042522 CC homozygous Human GRN RF 32972771
2219 Frontotemporal Lobar Degeneration SNP rs1990622 Human GRN RF more common (T) allele 20154673
2808 Frontotemporal Lobar Degeneration SNP rs5848 Human GRN RF Genotype:TT 18723524
1934 Alzheimer's Disease SNP rs5848 T allele Human GRN RF 26820675
3815 Lewy Body Disease SNP rs5848 Human GRN RF 34854996
2798 Amyotrophic Lateral Sclerosis SNP H63D(rs1799945) Human HFE RF Genotype:GC 20642794
2845 Amyotrophic Lateral Sclerosis SNP H63D(rs1799946) Human HFE RF Genotype:GC/GG 20642794
683 Parkinson disease SNP Cys282Tyr SNP Human HFE PF Australian PD patients 12098643
2874 Amyotrophic Lateral Sclerosis SNP H63D(rs1799947) Human HFE RF Genotype:G allele frequency 20642794
684 Parkinson disease SNP Cys282Tyr SNP Human HFE PF Australian PD patients 12098643
3268 Alzheimer's Disease SNP rs2075650 Human HIF3A RF eQTL(expression quantitative trait loci) analysis for the five SNPs closely related to AD 30319691
2338 Frontotemporal Lobar Degeneration SNP rs17219281 Human HLA-DQA2 RF Replication stage 30739198
2486 Frontotemporal Lobar Degeneration SNP rs17219281 Human HLA-DQA2 RF Discovery stage 30739198
3269 Parkinson disease SNP rs3129882 polymorphism Human HLA-DRA RF 25319953
2738 Amyotrophic Lateral Sclerosis SNP rs9268856 Human HLA-DRA/HLA-DRB5 RF the AA genotype at rs9268856 28131168
1931 Alzheimer's Disease SNP the C allele at rs9271192 Human HLA-DRB1 RF non-APOE ε4 carriers with rs9271192 genotype CC;additive model 29190991
2667 Alzheimer's Disease SNP the C allele at rs9271192 Human HLA-DRB1 RF non-APOE ε4 carriers with rs9271192 genotype CC;recessive model 29190991
533 Frontotemporal Lobar Degeneration SNP rs61831315 Human HMCN1 PF Discovery stage 30739198
2597 Frontotemporal Lobar Degeneration SNP rs7967622 Human hnRNP-A1 RF C/C genotype 21548758
2217 Frontotemporal Lobar Degeneration SNP rs7967622 Human hnRNP-A1 RF C/C genotype 21548758
554 Alzheimer's Disease SNP rs1008438 Human HSP70/HSPA1A PF Genotype: A/C; AD without depression 29703883
3272 Parkinson disease SNP Promoter -819 T/C polymorphism Human IL-10 RF 22387064
3271 Parkinson disease SNP Promoter -819 T/C polymorphism Human IL-10 RF 21241672
3273 Parkinson disease SNP 607C/A (rs1946518) polymorphism Human IL-18 RF 21241672
3275 Alzheimer's Disease SNP rs1800587 polymorphism Human IL-1B RF 26768592
3274 Alzheimer's Disease SNP rs1143634 polymorphism Human IL-1B RF 26768592
3276 Alzheimer's Disease SNP rs1800587 ? 889C > T Human IL-1α RF 27014584
3277 Multiple System Atrophy SNP rs16944 Human IL-1β RF 29251119
2201 Frontotemporal Lobar Degeneration SNP rs10267171 Human IMMP2L RF Discovery stage 30739198
2764 Amyotrophic Lateral Sclerosis SNP rs79609816 T Allele Human INPP5B RF 34421992
2280 Alzheimer's Disease SNP rs3781239 C allele Human insulin degrading enzyme gene (IDE) RF 20880607
2997 Alzheimer's Disease SNP CC genotypes Human insulin degrading enzyme gene (IDE) RF CC genotype was significantly associated with earlier age at onset 20880607
2832 Amyotrophic Lateral Sclerosis SNP rs4363506 and rs16984239 Human Intergenic RF The estimations using the proposed method (unadjusted estimates) 19740415
2787 Amyotrophic Lateral Sclerosis SNP rs4363506 and rs16984239 Human Intergenic RF The estimations using the proposed method (adjusted estimates) 19740415
2880 Amyotrophic Lateral Sclerosis SNP rs4363506 and rs3733242 Human Intergenic and SHROOM3 RF The estimations using the proposed method (unadjusted estimates) 19740415
2838 Amyotrophic Lateral Sclerosis SNP rs4363506 and rs3733242 Human Intergenic and SHROOM4 RF The estimations using the proposed method (adjusted estimates) 19740415
696 Frontotemporal Lobar Degeneration SNP rs11132244 Human IRF2 PF Discovery stage 30739198
2360 Alzheimer's Disease SNP rs1143676 Human ITGA4 RF Codominant; Genotype/Allele: AG; Univariate analysis 29769839
2242 Alzheimer's Disease SNP rs1143676 Human ITGA4 RF Overdominant; Genotype/Allele: AG; Multivariate analysis 29769839
2334 Alzheimer's Disease SNP rs1143676 Human ITGA4 RF Overdominant; Genotype/Allele: AG; Univariate analysis 29769839
2302 Alzheimer's Disease SNP rs1143676 Human ITGA4 RF Dominant; Genotype/Allele: AG+GG; Univariate analysis 29769839
2256 Alzheimer's Disease SNP rs1143676 Human ITGA4 RF Dominant; Genotype/Allele: AG+GG; Multivariate analysis 29769839
3278 Amyotrophic Lateral Sclerosis SNP rs2306677 Human ITPR2 RF 25023141
2181 Alzheimer's Disease SNP rs928771 Human KCNJ15 RF 29432188
574 Alzheimer's Disease SNP rs17070145 polymorphism Human KIBRA PF 24190487
3279 Alzheimer's Disease SNP rs6850306 Human LCORL RF 29860282
2108 Alzheimer's Disease SNP rs688T/T genotype Human LDLR RF 18065781
2149 Alzheimer's Disease SNP rs7707505 Human LOC100505811 RF 29027019
2091 Alzheimer's Disease SNP rs7723042 Human LOC100505811 RF 29027019
2183 Alzheimer's Disease SNP rs7729428 Human LOC100505811 RF 29027019
2180 Alzheimer's Disease SNP rs7729996 Human LOC100505811 RF 29027019
2105 Frontotemporal Lobar Degeneration SNP rs6463679 Human LOC101927354 RF Discovery stage 30739198
2526 Amyotrophic Lateral Sclerosis SNP rs3849942 Human LOC107987057 RF 20801718
1960 Amyotrophic Lateral Sclerosis SNP rs3849942 Human LOC107987057 RF In the joint analysis 20801717
2061 Amyotrophic Lateral Sclerosis SNP rs3849942 Human LOC107987057 RF 20801717
2057 Amyotrophic Lateral Sclerosis SNP rs2814707 Human LOC107987057,LOC112268043 RF 20801717
1961 Amyotrophic Lateral Sclerosis SNP rs2814707 Human LOC107987057,LOC112268043 RF In the joint analysis 20801717
2520 Amyotrophic Lateral Sclerosis SNP rs2814707 Human LOC112268043,LOC107987057 RF 20801718
2052 Alzheimer's Disease SNP allele (A) of the rs3755166 polymorphism Human LRP2 RF 20971101
805 Parkinson disease SNP SNPs in rs10878226 Human LRRK2 PF 23115130
3874 Parkinson disease SNP rs1491942 Human LRRK2 RF 33574311
1719 Parkinson disease SNP rs34778348 G2385R variant Human LRRK2 RF 35733392
1941 Parkinson disease SNP SNPs in rs10878226 Human LRRK2 RF 23115130
2682 Parkinson disease SNP G2385R (c.7153G>A) Human LRRK2 RF 17314670
3711 Alzheimer's Disease SNP rs4768231,rs4767971,rs7307310,rs1465527 Human LRRK2 RF 34135785
2491 Amyotrophic Lateral Sclerosis SNP rs7403881 Human M1(C/C) RF 17503480
555 Amyotrophic Lateral Sclerosis SNP rs1875233 Human M5(A/A) PF 17503480
2908 Amyotrophic Lateral Sclerosis SNP rs2291957 Human M6(T/T) RF 17503480
2379 Multiple System Atrophy SNP rs1052553 Human MAPT RF H1 haplotype 21321341
498 Progressive Supranuclear Palsy SNP rs8070723 Human MAPT PF 33897612
618 Progressive Supranuclear Palsy SNP rs242557 Human MAPT PF Meta-analysis 29986742
3037 Progressive Supranuclear Palsy SNP rs8070723 Human MAPT RF Meta-analysis 29986742
2582 Progressive Supranuclear Palsy SNP rs242557 Human MAPT RF 33897612
2783 Frontotemporal Lobar Degeneration SNP p.A152T Human MAPT RF 22556362
3288 Frontotemporal Lobar Degeneration SNP Human MFSD8 RF 30382371
3665 Amyotrophic Lateral Sclerosis SNP c.695T> C(p.L232P) Human MFSD8 RF 33226711
796 Alzheimer's Disease SNP rs242557 G/A polymorphism Human microtubule-associated protein tau (MAPT) gene PF individuals with a GG genotype of rs242557G/A 29098924
2129 Frontotemporal Lobar Degeneration SNP rs4240777 Human MIR548AP RF Discovery stage 30739198
3290 Alzheimer's Disease SNP Human MLKL RF MLKL loss-of-function mutation 29656768
2554 Amyotrophic Lateral Sclerosis SNP rs2225389 Human MOB3B RF 20801718
3291 Amyotrophic Lateral Sclerosis SNP rs2225389 Human MOB3B RF 25023141
3786 Amyotrophic Lateral Sclerosis SNP rs616147 polymorphism Human MOBP RF Greece 34694630
715 Progressive Supranuclear Palsy SNP rs1768208 Human MOBP PF Meta-analysis 29986742
2840 Parkinson disease SNP rs1799836 G allele polymorphism Human Monoamine oxidase-B (MAO-B) RF levodopa-induced dyskinesia(LID) 32346620
1888 Alzheimer's Disease SNP rs670139 (G>T) Human MS4A4E RF 26770425
3293 Alzheimer's Disease SNP rs610932 C allele Human MS4A6A RF 22382309
802 Alzheimer's Disease SNP rs610932 (G>T) Human MS4A6A PF 26770425
1857 Alzheimer's Disease SNP rs610932 Human MS4A6A RF Calculated by fixed effect model 29504051
1862 Alzheimer's Disease SNP rs610932 Human MS4A6A RF Calculated by fixed effect model 29504051
1861 Alzheimer's Disease SNP rs610932 Human MS4A6A RF Calculated by fixed effect model 29504051
2331 Alzheimer's Disease SNP rs11754661 polymorphism A allele Human MTHFD1L RF the results were influenced by APOE status 21741665
3294 Alzheimer's Disease SNP both rs1801133 T and rs1800795 C alleles Human MTHFR RF increased the odds of developing AD by 2.5 22015309
1937 Alzheimer's Disease SNP C677T allele Human MTHFR RF in APOE?4 or in non-APOE?4 carriers 28211809
2648 Amyotrophic Lateral Sclerosis SNP rs1801133 Human MTHFR(T677T) RF 22385294
2748 Amyotrophic Lateral Sclerosis SNP Human MTHFR(T677T/A1298A) RF 22385294
3295 Alzheimer's Disease SNP rs12506228A Human MTNR1A RF 29982836
2639 Parkinson disease SNP rs3738128 Human MUL1 RF 34946922
2071 Alzheimer's Disease SNP rs6797911 Human NEP gene (MME) RF 22493749
575 Alzheimer's Disease SNP Homozygosity of rs11833579 SNP Human NINJ2 PF 21674003
541 Alzheimer's Disease SNP Homozygosity of rs12425791 SNP Human NINJ2 PF 21674003
2226 Frontotemporal Lobar Degeneration SNP G894T (Glu298Asp) Human NOS3 RF 19087148
2304 Alzheimer's Disease SNP Human NT-3 RF homozygotes or heterozygotes for the mutated type (Glu[-63]) 9502217
599 Alzheimer's Disease SNP rs6489630 T allele Human NTF-3 PF in patients lacking the ApoE-?4 allele 26814132
2287 Frontotemporal Lobar Degeneration SNP rs13283101 Human OLFM1 RF Discovery stage 30739198
3085 Parkinson disease SNP IVS5+29T>A variant Human Omi/HTRA2 RF 21338583
2036 Alzheimer's Disease SNP rs1497525 Human OR2B2 RF 33654092
3300 Alzheimer's Disease SNP rs2653349(GA+AA) genotype Human OX2R RF A allele may be a susceptible factor for AD 30955315
3301 Alzheimer's Disease SNP rs2292041 A allele Human OX2R RF A allele may be a susceptible factor for AD 30955315
3137 Alzheimer's Disease SNP rs1050283 SNP Human oxidized LDL receptor 1(OLR1) RF 21709374
3126 Alzheimer's Disease SNP rs1050283 SNP Human oxidized LDL receptor 1(OLR1) RF 21709374
3302 Parkinson disease SNP Receptors gene 1513A>C polymorphism Human P2X7 RF 23648388
3303 Amyotrophic Lateral Sclerosis SNP rs145209834,rs138621837,rs200458051,rs200655529,rs143647285 Human P4HB/PDIA1 RF 25913742
3851 Parkinson disease SNP rs11240572 Human PARK16 RF 34373950
3304 Parkinson disease SNP rs823128, rs823156, and rs11240572 Human PARK16 RF 27174169
2396 Parkinson disease SNP rs947211 G/G genotype Human PARK16 RF 21419001
728 Parkinson disease SNP rs947211 Human PARK16 PF 27174169
1853 Tourette Syndrome SNP rs17371795 Human PCNT RF 32099372
1855 Tourette Syndrome SNP rs2839228 Human PCNT RF 32099372
1852 Tourette Syndrome SNP rs2839227 Human PCNT RF 32099372
2103 Alzheimer's Disease SNP G523A A allele Human PEMT RF 21881829
2545 Amyotrophic Lateral Sclerosis SNP rs140547520 Human PFN1 RF 24309268
2352 Alzheimer's Disease SNP rs561655 Human PICALM RF PENN cohort 30128317
2508 Alzheimer's Disease SNP rs3851179 Human PICALM RF PENN cohort 30128317
752 Parkinson disease SNP rs28499371 T allele Human PLEKHN1 PF 33510632
832 Alzheimer's Disease SNP Human PM20D1 PF in a particular genetic background 29736028
3995 Charcot-Marie-Tooth (CMT) disease SNP T118M variation Human PMP22 RF 36581210
2390 Amyotrophic Lateral Sclerosis SNP rs662 Human PON1 Q192R(major allele is Q) RF Recessive (RR vs other) 16822965
2086 Amyotrophic Lateral Sclerosis SNP rs662 Human PON1 Q192R(major allele is Q) RF Additive 16822965
2132 Amyotrophic Lateral Sclerosis SNP rs6954345 Human PON2 C311S (major allele is S) RF Dominant (CC and CS vs SS) 16822965
2046 Amyotrophic Lateral Sclerosis SNP rs6954345 Human PON2 C311S (major allele is S) RF Additive 16822965
2484 Creutzfeldt-Jakob disease SNP rs2756271 Human PRNP RF 22210626
2918 Creutzfeldt-Jakob disease SNP rs6107516 Human PRNP RF 19081515
2882 Creutzfeldt-Jakob disease SNP rs6116492 Human PRNP RF 19081515
3004 Creutzfeldt-Jakob disease SNP M129V MM heterozygote Human PRNP RF 34831353
2166 Creutzfeldt-Jakob disease SNP rs638405 Human PRNP RF BACE1?C-allele carriers 22952813
2405 Creutzfeldt-Jakob disease SNP rs638405 Human PRNP RF BACE1?C-allele carriers 22952813
3318 Alzheimer's Disease SNP Human PS-1 RF 9298817
3928 Alzheimer's Disease SNP rs756609078 Thr421Met Human PSEN2 RF 36362122
763 Alzheimer's Disease SNP rs28834970 Human PTK2B PF National Alzheimer’s Coordinating Center (NACC) cohort 30128317
3791 Amyotrophic lateral sclerosis,Parkinson disease SNP rs6030462 Human PTPRT RF 34707478
1573 Alzheimer's Disease SNP rs6859 Human PVRL2 RF using Cox regression、Dataset：CHS（Cardiovascular Health Study） 29107063
3324 Alzheimer's Disease SNP rs2075650 Human PVRL2 RF eQTL(expression quantitative trait loci) analysis for the five SNPs closely related to AD 30319691
2261 Alzheimer's Disease SNP rs6859 Human PVRL2 RF using logistic regression、Dataset：LOADFS(Late Onset Alzheimer's Disease Family Study ) 29107063
2114 Alzheimer's Disease SNP rs283815 Human PVRL2 RF using logistic regression、Dataset：HRS(Health and Retirement Study) 29107063
2064 Alzheimer's Disease SNP rs6859 Human PVRL2 RF using logistic regression、Dataset：CHS( Cardiovascular Health Study) 29107063
3323 Alzheimer's Disease SNP rs769449 Human PVRL2 RF eQTL(expression quantitative trait loci) analysis for the five SNPs closely related to AD 30319691
3325 Alzheimer's Disease SNP rs157580 Human PVRL2 RF eQTL(expression quantitative trait loci) analysis for the five SNPs closely related to AD 30319691
2058 Alzheimer's Disease SNP A80G GG genotype Human reduced folate carrier gene (RFC1) RF especially for female individuals 18258338
2019 Alzheimer's Disease SNP A80G G allele Human reduced folate carrier gene (RFC1) RF especially for female individuals 18258338
700 Frontotemporal Lobar Degeneration SNP rs12425381 Human RERG PF Discovery stage 30739198
3329 Parkinson disease SNP rs62063857 AA genotype Human Saitohin RF 25168738
833 Parkinson disease SNP rs62063857 AG genotype Human Saitohin PF 25168738
798 Parkinson disease SNP rs7702187 polymorphism Human SEMA5A PF 24706317
3106 Alzheimer's Disease SNP rs1799889 4G/4G genotype Human SERPINE1 RF women were at an increased risk over their male genotype counterparts 28466654
2965 Alzheimer's Disease SNP rs1799889 4G/5G genotype Human SERPINE1 RF women were at an increased risk over their male genotype counterparts 28466654
3052 Alzheimer's Disease SNP rs572750141 variant (NM_030974.3:p.Gly186Arg) Human SHARPIN RF 31216982
2227 Alzheimer's Disease SNP rs10410544 T allele Human SIRT2 RF APOEε4 noncarriers 24139700
3332 Alzheimer's Disease SNP rs10410544 C/T polymorphism Human SIRT2 RF 24139700
1982 Parkinson disease SNP Genotype allele G of the promoter SNP rs2652510 Human SLC6A3 RF 24211691
2051 Parkinson disease SNP Genotype GG of the promoter SNP rs2652510 Human SLC6A3 RF 24211691
1981 Parkinson disease SNP Genotype allele G of the promoter SNP rs2652510 Human SLC6A3 RF 24211691
2050 Parkinson disease SNP Genotype GG of the promoter SNP rs2652510 Human SLC6A3 RF 24211691
578 Alzheimer's Disease SNP rs4795541 Human SLC6A4/5-HTT PF S allele; AD with depression 29703883
709 Progressive Supranuclear Palsy SNP rs11568563 Human SLCO1A2 PF Meta-analysis 29986742
3994 Spinal muscular atrophy (SMA) SNP rs121909192 Human SMN1 RF 37964750
708 Parkinson disease SNP rs11931074 Human SNCA PF 34946922
2047 Lewy Body Disease SNP rs7681440 Human SNCA RF 34308904
742 Dementia with Lewy bodies SNP rs7681440; Human SNCA PF 29263008
3142 Parkinson disease SNP rs356220, rs356203, rs7684318 and rs2736990 polymorphism Human SNCA RF 27699750
2357 Parkinson disease SNP rs356219 variant Human SNCA RF 22349157
3129 Parkinson disease SNP rs7684318 C-allele Human SNCA RF 33705925
590 Alzheimer's Disease SNP rs2070424 Human SOD1 gene PF Logistic regression analysis controlled for age, genderand APOE carrier status；recessive model 25440013
627 Alzheimer's Disease SNP rs2070424 Human SOD1 gene PF After Bonferroni correction；additive model 25440013
589 Alzheimer's Disease SNP rs2070424 Human SOD1 gene PF Logistic regression analysis controlled for age, genderand APOE carrier status；additive model 25440013
637 Alzheimer's Disease SNP rs2070424 Human SOD1 gene PF After Bonferroni correction；recessive model 25440013
3916 Alzheimer's Disease SNP NM_003105.6: c.4519+5G>A Human SORL1 RF 35457051
2404 Alzheimer's Disease SNP SNP rs985421 A allele Human SORL1 RF 24486888
3706 Alzheimer's Disease SNP rs3737529 Human SORL1 RF 34214049
834 Alzheimer's Disease SNP Human SORL1 PF 18407551
3908 Alzheimer's Disease SNP rs1784933 A/A genotype Human SORL1 RF 35456392
2059 Alzheimer's Disease SNP rs641120 Human SORL1 RF adjusted for age and gender 25881907
2053 Alzheimer's Disease SNP rs641120 Human SORL1 RF adjusted foe age, gender, APOE 4 25881907
3915 Alzheimer's Disease SNP rs775517202 c.364C>T Human SORL1 RF 35457051
3337 Alzheimer's Disease SNP rs1784933 Human SORL1 RF with the A allele 25450149
823 Alzheimer's Disease SNP Human SORL1 PF 30009200
674 Alzheimer's Disease SNP rs17646665 GA Genotype Human SORT1 PF 27392867
3341 Alzheimer's Disease SNP rs2269657 Human SREBF2 RF significant dual associations with LOAD pathological biomarkers and gene expression levels 29503034
2529 Alzheimer's Disease SNP rs10164112-T allele Human STARD6 RF in combination with the APOE ε4 allele 30666118
2218 Parkinson disease SNP rs1955337 TT genotype Human STK39 RF 26469904
775 Progressive Supranuclear Palsy SNP rs1411478 Human STX6 PF Meta-analysis 29986742
3343 Amyotrophic Lateral Sclerosis SNP rs2708909 Human SUN3, HUS1 RF 25023141
3344 Alzheimer's Disease SNP rs4420638 Human SYMPK RF eQTL(expression quantitative trait loci) analysis for the five SNPs closely related to AD 30319691
3345 Amyotrophic Lateral Sclerosis SNP rs80356717 Human TARDBP RF 25023141
3346 Frontotemporal Lobar Degeneration SNP c.269C>T (p.A90V) Human TARDBP RF 18505686
2310 Parkinson disease SNP rs2306604 G/G genotype Human TFAM RF 19925850
2311 Alzheimer's Disease SNP rs1982073 Human TGF-β1 RF without the ApoE ε4 allele;G 26327336
2363 Alzheimer's Disease SNP rs1982073 Human TGF-β1 RF without the ApoE ε4 allele;TG 26327336
2081 Alzheimer's Disease SNP rs1982073 Human TGF-β1 RF allele G 26327336
2238 Alzheimer's Disease SNP rs1800469 Human TGF-β1 RF allele C 26327336
2160 Alzheimer's Disease SNP rs1800469 Human TGF-β1 RF without the ApoE ε4allele;C 26327336
2229 Alzheimer's Disease SNP rs1982073 Human TGF-β1 RF Genotype TG 26327336
2472 Alzheimer's Disease SNP rs1800469 Human TGF-β1 RF Genotype AC 26327336
2713 Alzheimer's Disease SNP rs1800469 Human TGF-β1 RF AC+ CC vs AA 26327336
2270 Alzheimer's Disease SNP rs1800469 Human TGF-β1 RF without the ApoE ε4 allele;AC 26327336
3352 Amyotrophic Lateral Sclerosis SNP rs13048019 Human TIAM1 RF 25023141
2481 Amyotrophic Lateral Sclerosis SNP rs13048019 Human TIAM1 RF 20801718
835 Alzheimer's Disease SNP minor alleles of seven SNPs (rs10759930, rs1927914, rs1927911, rs12377632, rs2149356, rs7037117, and rs7045953) Human TLR4 PF when incorporated into a haplotype with rs10759930, the strongest association was detected 22272615
2479 Frontotemporal Lobar Degeneration SNP rs3849942 Human TMEM106B RF for chromosome 9 SNP association; Denotes the associated SNP’s from the GWAS. 21257233
837 Frontotemporal Dementia SNP rs1990622 Human TMEM106B PF C9ORF72 expansion carriers;Cohort 1 – controls and C9ORF72 repeat expansion carriers (FTD, FTD/MND, and MND, or other diagnosis) 24385136
3814 Lewy Body Disease SNP rs1990622 Human TMEM106B RF 34854996
2512 Frontotemporal Lobar Degeneration SNP rs10812605 Human TMEM106B RF for chromosome 9 SNP association 21257233
2235 Frontotemporal Lobar Degeneration SNP rs2015747 Human TMEM106B RF for chromosome 1 SNP association 21257233
2318 Frontotemporal Lobar Degeneration SNP rs774351 Human TMEM106B RF for chromosome 9 SNP association; Denotes the associated SNP’s from the GWAS. 21257233
662 Frontotemporal Lobar Degeneration SNP rs1990622 Human TMEM106B PF GRN carriers 25085782
2489 Frontotemporal Lobar Degeneration SNP rs868856 Human TMEM106B RF for chromosome 9 SNP association 21257233
2942 Frontotemporal Lobar Degeneration SNP rs12350089 Human TMEM106B RF for chromosome 9 SNP association 21257233
668 Frontotemporal Lobar Degeneration SNP rs2015747 Human TMEM106B PF for SNPs on chromosomes 1, 8, 10 and 11 genotyped 21257233
3777 Amyotrophic Lateral Sclerosis SNP rs1990622 A/A Human TMEM106B RF 33314436
836 Frontotemporal Dementia SNP rs3173615 Human TMEM106B PF C9ORF72 expansion carriers;Cohort 1 – controls and C9ORF72 repeat expansion carriers (FTD, FTD/MND, and MND, or other diagnosis) 24385136
2553 Frontotemporal Lobar Degeneration SNP rs2814707 Human TMEM106B RF for chromosome 9 SNP association; Denotes the associated SNP’s from the GWAS;Denotes the associated SNP’s from the ALS GWAS 21257233
3798 Frontotemporal Lobar Degeneration SNP rs1990622 A/A genotype Human TMEM106B RF 33314436
2317 Frontotemporal Lobar Degeneration SNP rs1565948 Human TMEM106B RF for chromosome 9 SNP association 21257233
2244 Frontotemporal Lobar Degeneration SNP rs10967976 Human TMEM106B RF for chromosome 9 SNP association 21257233
2549 Frontotemporal Lobar Degeneration SNP rs10967959 Human TMEM106B RF for chromosome 9 SNP association 21257233
1849 Frontotemporal Lobar Degeneration SNP rs2015747 Human TMEM106B RF for chromosome 1 SNP association 21257233
2607 Frontotemporal Lobar Degeneration SNP rs774352 Human TMEM106B RF for chromosome 9 SNP association; Denotes the associated SNP’s from the GWAS. 21257233
3353 Alzheimer's Disease SNP rs1990622 polymorphism Human TMEM106B RF APOE interact 24166182
3354 Alzheimer's Disease SNP rs12435391（IVS4-28T> C） Human TMP21 RF 28233271
2358 Multiple System Atrophy SNP rs1799964 Human TNF-α RF allele 29251119
1968 Multiple System Atrophy SNP rs1799964 Human TNF-α RF genotype 29251119
2885 Alzheimer's Disease SNP rs10119 GG genotype Human TOMM40 RF APOE ε4+ 32725468
2564 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using logistic regression、Dataset：CHS( Cardiovascular Health Study) 29107063
690 Alzheimer's Disease SNP rs157580 A allele Human TOMM40 PF the association between the Asian and Caucasian groups was significantly different 26795201
2735 Alzheimer's Disease SNP rs2075650 A allele Human TOMM40 RF the association between the Asian and Caucasian groups was significantly different 26795201
2115 Alzheimer's Disease SNP rs157582 Human TOMM40 RF using logistic regression、Dataset：HRS(Health and Retirement Study) 29107063
3356 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF 29797398
1589 Alzheimer's Disease SNP rs71352238 Human TOMM40 RF using Cox regression、Dataset：HRS（Health and Retirement Study） 29107063
1621 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using Cox regression、Dataset：FHS（Framingham Heart Study） 29107063
2565 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using logistic regression、Dataset：FHS(Framingham Heart Study) 29107063
1588 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using Cox regression、Dataset：HRS（Health and Retirement Study） 29107063
3696 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF 34336000
2184 Alzheimer's Disease SNP rs71352238 Human TOMM40 RF using logistic regression、Dataset：HRS(Health and Retirement Study) 29107063
2964 Alzheimer's Disease SNP rs71352238 CT genotype Human TOMM40 RF APOE ε4+ 32725468
2116 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using logistic regression、Dataset：HRS(Health and Retirement Study) 29107063
3357 Alzheimer's Disease SNP rs157580 Human TOMM40 RF 29797398
2896 Alzheimer's Disease SNP rs71352238 TT genotype Human TOMM40 RF APOE ε4+ 32725468
2935 Alzheimer's Disease SNP rs10119 AG genotype Human TOMM40 RF APOE ε4+ 32725468
1673 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using Cox regression、Dataset：CHS（Cardiovascular Health Study） 29107063
2862 Alzheimer's Disease SNP rs2075650 Human TOMM40 RF using logistic regression、Dataset：LOADFS(Late Onset Alzheimer's Disease Family Study ) 29107063
2445 Alzheimer's Disease SNP rs10119 AA genotype Human TOMM40 RF APOE ε4+ 32725468
1488 Frontotemporal Dementia SNP rs1042522 Human TP53 RF 32972771
3011 Frontotemporal Dementia SNP rs75932628(p.R47H) Human TREM2 RF 23800361
3360 Alzheimer's Disease SNP rs75932628 Human TREM2 RF 29794134
2679 Frontotemporal Lobar Degeneration SNP rs2234253 Human TREM2 RF carrier T vs. G 29322490
3366 Frontotemporal Lobar Degeneration SNP rs754650868 Human TREM2 RF 29557178
2703 Alzheimer's Disease SNP rs75932628 Human TREM2 RF 26037549
2928 Alzheimer's Disease SNP rs75932628(T variant ) Human TREM2 RF 23380991
2609 Amyotrophic Lateral Sclerosis SNP rs75932628 Human TREM2 RF 24535663
3363 Frontotemporal Lobar Degeneration SNP rs201258314 Human TREM2 RF Compound heterozygosity 29557178
2681 Frontotemporal Lobar Degeneration SNP rs2234253 Human TREM2 RF GT+TT vs. GG 29322490
2933 Alzheimer's Disease SNP rs75932628-T(p.R47H) variant Human TREM2 RF 24041969
2534 Alzheimer's Disease SNP p.R47H (rs75932628) Human TREM2 RF 25160042
2617 Frontotemporal Lobar Degeneration SNP rs75932628 Human TREM2 RF T vs. C 29322490
2427 Alzheimer's Disease SNP rs75932628 Human TREM2 RF the T allele of the rs75932628 variant of TREM2 25260849
3359 Alzheimer's Disease SNP rs75932628 Human TREM2 RF 30222607
2559 Frontotemporal Lobar Degeneration SNP rs75932628 Human TREM2 RF CT vs. CC 29322490
2678 Frontotemporal Lobar Degeneration SNP rs2234253 Human TREM2 RF T vs. G 29322490
3365 Frontotemporal Lobar Degeneration SNP rs201258663 Human TREM2 RF Compound heterozygosity 29557178
3012 Frontotemporal Lobar Degeneration SNP rs75932628 Human TREM2 RF 23800361
3362 Frontotemporal Lobar Degeneration SNP Human TREM2 RF A large consanguineous Colombian family segregating autosomal recessive FTLD 23582655
2680 Frontotemporal Lobar Degeneration SNP rs2234253 Human TREM2 RF GT vs. GG 29322490
3367 Frontotemporal Lobar Degeneration SNP rs142232675 Human TREM2 RF Homozygosity 29557178
2704 Alzheimer's Disease SNP rs75932628 Human TREM2 RF 25936935
2932 Alzheimer's Disease SNP rs75932628-T(p.R47H) variant Human TREM2 RF 24041969
2849 Alzheimer's Disease SNP rs75932628 (R47H) variant Human TREM2 RF 23855982
2558 Frontotemporal Lobar Degeneration SNP rs75932628 Human TREM2 RF CT+TT vs. CC 29322490
3364 Frontotemporal Lobar Degeneration SNP rs143332484 Human TREM2 RF 29557178
2552 Frontotemporal Lobar Degeneration SNP rs75932628 Human TREM2 RF carrier T vs. C 29322490
2958 Multiple System Atrophy SNP rs75932628 Human TREM2 p.R47H RF patients with pathologically confirmed MSA 30109269
1817 Multiple System Atrophy SNP rs75932628 Human TREM2 p.R47H RF patients with pathologically confirmed MSA 30109269
1813 Multiple System Atrophy SNP rs75932628 Human TREM2 p.R47H RF patients with clinically diagnosed MSA 30109269
2893 Multiple System Atrophy SNP rs75932628 Human TREM2 p.R47H RF patients with clinically diagnosed MSA 30109269
2173 Parkinson disease SNP AA genotype of UCHL1 S18Y SNP Human UCHL1 RF 22839974
2171 Frontotemporal Lobar Degeneration SNP rs12973192 Human UNC13A RF Replication stage 30739198
1904 Amyotrophic Lateral Sclerosis SNP rs12608932 Human UNC13A RF especially in Caucasian and European subjects 31201598
2099 Frontotemporal Lobar Degeneration SNP rs12973192 Human UNC13A RF Discovery stage 30739198
2049 Frontotemporal Lobar Degeneration SNP -2578 C/A Human VEGF RF A allele 18729809
2112 Parkinson disease SNP rs3025039 polymorphism Human VEGF RF 27481110
2020 Frontotemporal Lobar Degeneration SNP -1154 G/A Human VEGF RF A allele 18729809
3853 Parkinson disease SNP FokI (rs2228570) T allele Human vitamin D Receptor(VDR) RF 34365149
3852 Parkinson disease SNP FokI (rs2228570) T allele and TT genotype Human vitamin D Receptor(VDR) RF 34365149
3854 Parkinson disease SNP rs1989969 GCTG haplotype Human vitamin D Receptor(VDR) RF 34365149
3371 Parkinson disease SNP rs363324 at -11.5 kb in the hVMAT2 promoter Human VMAT2 RF 27137201
740 Parkinson disease SNP rs863108 T allele Human ZFP64/TSHZ2 PF 33510632
3779 Amyotrophic Lateral Sclerosis SNP rs2275294-C allele Human ZNF512B RF 33387304
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