rs61497286
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61497286(C;T) |
Make rs61497286(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 17 |
Position | 44913318 |
Gene | GFAP |
is a | snp |
is | mentioned by |
dbSNP | rs61497286 |
dbSNP (classic) | rs61497286 |
ClinGen | rs61497286 |
ebi | rs61497286 |
HLI | rs61497286 |
Exac | rs61497286 |
Gnomad | rs61497286 |
Varsome | rs61497286 |
LitVar | rs61497286 |
Map | rs61497286 |
PheGenI | rs61497286 |
Biobank | rs61497286 |
1000 genomes | rs61497286 |
hgdp | rs61497286 |
ensembl | rs61497286 |
geneview | rs61497286 |
scholar | rs61497286 |
rs61497286 | |
pharmgkb | rs61497286 |
gwascentral | rs61497286 |
openSNP | rs61497286 |
23andMe | rs61497286 |
SNPshot | rs61497286 |
SNPdbe | rs61497286 |
MSV3d | rs61497286 |
GWAS Ctlg | rs61497286 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61497286(T;T) |
Alt | rs61497286(T;T) |
Reference | Rs61497286(C;C) |
Significance | Pathogenic |
Disease | not provided Alexander's disease |
Variation | info |
Gene | GFAP |
CLNDBN | not provided Alexander's disease |
Reversed | 1 |
HGVS | NC_000017.10:g.42990686G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000056903.1, RCV000192139.1, |