rs782090947
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;G) | 3 | Carrier of G6PD deficiency mutation; variable expressivity |
(G;G) | 5 | G6PD deficiency |
is a | snp |
is | mentioned by |
dbSNP | rs782090947 |
dbSNP (classic) | rs782090947 |
ClinGen | rs782090947 |
ebi | rs782090947 |
HLI | rs782090947 |
Exac | rs782090947 |
Gnomad | rs782090947 |
Varsome | rs782090947 |
LitVar | rs782090947 |
Map | rs782090947 |
PheGenI | rs782090947 |
Biobank | rs782090947 |
1000 genomes | rs782090947 |
hgdp | rs782090947 |
ensembl | rs782090947 |
geneview | rs782090947 |
scholar | rs782090947 |
rs782090947 | |
pharmgkb | rs782090947 |
gwascentral | rs782090947 |
openSNP | rs782090947 |
23andMe | rs782090947 |
SNPshot | rs782090947 |
SNPdbe | rs782090947 |
MSV3d | rs782090947 |
GWAS Ctlg | rs782090947 |
Max Magnitude | 5 |
aka c.209A>G (p.Tyr70Cys)