rs387906468
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 5 | G6PD deficiency |
(A;G) | 3 | Carrier of G6PD deficiency mutation; variable expressivity |
(G;G) | 0 | common/normal |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 154532752 |
Gene | G6PD |
is a | snp |
is | mentioned by |
dbSNP | rs387906468 |
dbSNP (classic) | rs387906468 |
ClinGen | rs387906468 |
ebi | rs387906468 |
HLI | rs387906468 |
Exac | rs387906468 |
Gnomad | rs387906468 |
Varsome | rs387906468 |
LitVar | rs387906468 |
Map | rs387906468 |
PheGenI | rs387906468 |
Biobank | rs387906468 |
1000 genomes | rs387906468 |
hgdp | rs387906468 |
ensembl | rs387906468 |
geneview | rs387906468 |
scholar | rs387906468 |
rs387906468 | |
pharmgkb | rs387906468 |
gwascentral | rs387906468 |
openSNP | rs387906468 |
23andMe | rs387906468 |
SNPshot | rs387906468 |
SNPdbe | rs387906468 |
MSV3d | rs387906468 |
GWAS Ctlg | rs387906468 |
Max Magnitude | 5 |