Have questions? Visit https://www.reddit.com/r/SNPedia

rs2230037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2230037(C;T)
Make rs2230037(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532439
GeneG6PD
is asnp
is mentioned by
dbSNPrs2230037
ebirs2230037
HLIrs2230037
Exacrs2230037
Varsomers2230037
Maprs2230037
PheGenIrs2230037
hapmaprs2230037
1000 genomesrs2230037
hgdprs2230037
ensemblrs2230037
gopubmedrs2230037
geneviewrs2230037
scholarrs2230037
googlers2230037
pharmgkbrs2230037
gwascentralrs2230037
openSNPrs2230037
23andMers2230037
23andMe allrs2230037
SNP Nexus

SNPshotrs2230037
SNPdbers2230037
MSV3drs2230037
GWAS Ctlgrs2230037
GMAF0.1385
Max Magnitude0


GET Evidence
rs2230037
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.165506
summary



ClinVar
Risk rs2230037(T;T)
Alt rs2230037(T;T)
Reference rs2230037(C;C)
Significance Non-pathogenic
Disease Glucose 6 phosphate dehydrogenase deficiency not specified
Variation info
Gene G6PD
CLNDBN Glucose 6 phosphate dehydrogenase deficiency not specified
Reversed 1
HGVS NC_000023.10:g.153760654G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000011084.4, RCV000079394.4,