Variant #0000001396 (NC_000017.10:g.42428532G>A, GRN(NM_002087.2):c.835+1G>A)
| Individual ID |
00001396 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42428532G>A |
| Reference |
Masellis M1, Momeni P, Meschino W, Heffner R Jr, Elder J, Sato C, Liang Y, St George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E.(2006) |
| DB-ID |
GRN_000054 See all 2 reported entries |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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