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rs1050757

From SNPedia

Orientationminus
Stabilizedminus
Make rs1050757(A;A)
Make rs1050757(A;G)
Make rs1050757(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154531643
GeneG6PD
is asnp
is mentioned by
dbSNPrs1050757
ebirs1050757
HLIrs1050757
Exacrs1050757
Varsomers1050757
Maprs1050757
PheGenIrs1050757
hapmaprs1050757
1000 genomesrs1050757
hgdprs1050757
ensemblrs1050757
gopubmedrs1050757
geneviewrs1050757
scholarrs1050757
googlers1050757
pharmgkbrs1050757
gwascentralrs1050757
openSNPrs1050757
23andMers1050757
23andMe allrs1050757
SNP Nexus

SNPshotrs1050757
SNPdbers1050757
MSV3drs1050757
GWAS Ctlgrs1050757
GMAF0.3108
Max Magnitude

[PMID 23389243] 3'-UTR variations and G6PD deficiency


[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.