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rs137852334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852334(C;T)
Make rs137852334(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532695
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852334
ebirs137852334
HLIrs137852334
Exacrs137852334
Varsomers137852334
Maprs137852334
PheGenIrs137852334
hapmaprs137852334
1000 genomesrs137852334
hgdprs137852334
ensemblrs137852334
gopubmedrs137852334
geneviewrs137852334
scholarrs137852334
googlers137852334
pharmgkbrs137852334
gwascentralrs137852334
openSNPrs137852334
23andMers137852334
23andMe allrs137852334
SNP Nexus

SNPshotrs137852334
SNPdbers137852334
MSV3drs137852334
GWAS Ctlgrs137852334
Max Magnitude0
OMIM305900
Desc
Variant0037
Relatedalso
ClinVar
Risk rs137852334(T;T)
Alt rs137852334(T;T)
Reference rs137852334(C;C)
Significance Other
Disease G6PD GUADALAJARA Anemia
Variation info
Gene G6PD
CLNDBN G6PD GUADALAJARA Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153760910G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011132.2, RCV000011133.6,