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rs137852337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852337(C;C)
Make rs137852337(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532434
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852337
ebirs137852337
HLIrs137852337
Exacrs137852337
Varsomers137852337
Maprs137852337
PheGenIrs137852337
hapmaprs137852337
1000 genomesrs137852337
hgdprs137852337
ensemblrs137852337
gopubmedrs137852337
geneviewrs137852337
scholarrs137852337
googlers137852337
pharmgkbrs137852337
gwascentralrs137852337
openSNPrs137852337
23andMers137852337
23andMe allrs137852337
SNP Nexus

SNPshotrs137852337
SNPdbers137852337
MSV3drs137852337
GWAS Ctlgrs137852337
Max Magnitude0
OMIM305900
Desc
Variant0040
Relatedalso
ClinVar
Risk rs137852337(A,C;A,C)
Alt rs137852337(A,C;A,C)
Reference rs137852337(G;G)
Significance Other
Disease G6PD PAWNEE Anemia
Variation info
Gene G6PD
CLNDBN G6PD PAWNEE Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153760649C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011138.3, RCV000011139.6,