rs112950723
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs112950723(C;C) |
Make rs112950723(C;T) |
Make rs112950723(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 154531728 |
Gene | G6PD |
is a | snp |
is | mentioned by |
dbSNP | rs112950723 |
dbSNP (classic) | rs112950723 |
ClinGen | rs112950723 |
ebi | rs112950723 |
HLI | rs112950723 |
Exac | rs112950723 |
Gnomad | rs112950723 |
Varsome | rs112950723 |
LitVar | rs112950723 |
Map | rs112950723 |
PheGenI | rs112950723 |
Biobank | rs112950723 |
1000 genomes | rs112950723 |
hgdp | rs112950723 |
ensembl | rs112950723 |
geneview | rs112950723 |
scholar | rs112950723 |
rs112950723 | |
pharmgkb | rs112950723 |
gwascentral | rs112950723 |
openSNP | rs112950723 |
23andMe | rs112950723 |
SNPshot | rs112950723 |
SNPdbe | rs112950723 |
MSV3d | rs112950723 |
GWAS Ctlg | rs112950723 |
Max Magnitude | 0 |
[PMID 23389243] 3'-UTR variations and G6PD deficiency