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rs137852336

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852336(A;A)
Make rs137852336(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532625
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852336
ebirs137852336
HLIrs137852336
Exacrs137852336
Varsomers137852336
Maprs137852336
PheGenIrs137852336
hapmaprs137852336
1000 genomesrs137852336
hgdprs137852336
ensemblrs137852336
gopubmedrs137852336
geneviewrs137852336
scholarrs137852336
googlers137852336
pharmgkbrs137852336
gwascentralrs137852336
openSNPrs137852336
23andMers137852336
23andMe allrs137852336
SNP Nexus

SNPshotrs137852336
SNPdbers137852336
MSV3drs137852336
GWAS Ctlgrs137852336
Max Magnitude0
OMIM305900
Desc
Variant0039
Relatedalso
ClinVar
Risk rs137852336(A;A)
Alt rs137852336(A;A)
Reference rs137852336(G;G)
Significance Other
Disease G6PD JAPAN Anemia
Variation info
Gene G6PD
CLNDBN G6PD JAPAN Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153760840C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011136.2, RCV000011137.5,