rs763868966
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs763868966(A;A) |
Make rs763868966(A;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 44911429 |
Gene | GFAP |
is a | snp |
is | mentioned by |
dbSNP | rs763868966 |
dbSNP (classic) | rs763868966 |
ClinGen | rs763868966 |
ebi | rs763868966 |
HLI | rs763868966 |
Exac | rs763868966 |
Gnomad | rs763868966 |
Varsome | rs763868966 |
LitVar | rs763868966 |
Map | rs763868966 |
PheGenI | rs763868966 |
Biobank | rs763868966 |
1000 genomes | rs763868966 |
hgdp | rs763868966 |
ensembl | rs763868966 |
geneview | rs763868966 |
scholar | rs763868966 |
rs763868966 | |
pharmgkb | rs763868966 |
gwascentral | rs763868966 |
openSNP | rs763868966 |
23andMe | rs763868966 |
SNPshot | rs763868966 |
SNPdbe | rs763868966 |
MSV3d | rs763868966 |
GWAS Ctlg | rs763868966 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763868966(A;A) rs763868966(T;T) |
Alt | rs763868966(A;A) rs763868966(T;T) |
Reference | Rs763868966(C;C) |
Significance | Other |
Disease | Alexander's disease |
Variation | info |
Gene | GFAP |
CLNDBN | Alexander's disease |
Reversed | 0 |
HGVS | NC_000017.10:g.42988797C>A |
CLNSRC | |
CLNACC | RCV000192151.1, |