rs797044432
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 8.8 | Tay-Sachs disease (predicted) |
(C;G) | 3 | Carrier of a Tay-Sachs mutation |
(G;G) | 0 | common in clinvar |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 72356524 |
Gene | HEXA |
is a | snp |
is | mentioned by |
dbSNP | rs797044432 |
dbSNP (classic) | rs797044432 |
ClinGen | rs797044432 |
ebi | rs797044432 |
HLI | rs797044432 |
Exac | rs797044432 |
Gnomad | rs797044432 |
Varsome | rs797044432 |
LitVar | rs797044432 |
Map | rs797044432 |
PheGenI | rs797044432 |
Biobank | rs797044432 |
1000 genomes | rs797044432 |
hgdp | rs797044432 |
ensembl | rs797044432 |
geneview | rs797044432 |
scholar | rs797044432 |
rs797044432 | |
pharmgkb | rs797044432 |
gwascentral | rs797044432 |
openSNP | rs797044432 |
23andMe | rs797044432 |
SNPshot | rs797044432 |
SNPdbe | rs797044432 |
MSV3d | rs797044432 |
GWAS Ctlg | rs797044432 |
Max Magnitude | 8.8 |
ClinVar | |
---|---|
Risk | Rs797044432(C;C) |
Alt | Rs797044432(C;C) |
Reference | Rs797044432(G;G) |
Significance | Other |
Disease | Tay-Sachs disease |
Variation | info |
Gene | HEXA |
CLNDBN | Tay-Sachs disease |
Reversed | 1 |
HGVS | NC_000015.9:g.72648865C>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000004097.2, |