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rs137852343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852343(C;C)
Make rs137852343(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154534465
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852343
ebirs137852343
HLIrs137852343
Exacrs137852343
Varsomers137852343
Maprs137852343
PheGenIrs137852343
hapmaprs137852343
1000 genomesrs137852343
hgdprs137852343
ensemblrs137852343
gopubmedrs137852343
geneviewrs137852343
scholarrs137852343
googlers137852343
pharmgkbrs137852343
gwascentralrs137852343
openSNPrs137852343
23andMers137852343
23andMe allrs137852343
SNP Nexus

SNPshotrs137852343
SNPdbers137852343
MSV3drs137852343
GWAS Ctlgrs137852343
Max Magnitude0
OMIM305900
Desc
Variant0048
Relatedalso
ClinVar
Risk rs137852343(C;C)
Alt rs137852343(C;C)
Reference rs137852343(T;T)
Significance Other
Disease G6PD NANKANG
Variation info
Gene G6PD
CLNDBN G6PD NANKANG
Reversed 1
HGVS NC_000023.10:g.153762680A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011150.1,