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rs137852322

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852322(C;C)
Make rs137852322(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532701
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852322
ebirs137852322
HLIrs137852322
Exacrs137852322
Varsomers137852322
Maprs137852322
PheGenIrs137852322
hapmaprs137852322
1000 genomesrs137852322
hgdprs137852322
ensemblrs137852322
gopubmedrs137852322
geneviewrs137852322
scholarrs137852322
googlers137852322
pharmgkbrs137852322
gwascentralrs137852322
openSNPrs137852322
23andMers137852322
23andMe allrs137852322
SNP Nexus

SNPshotrs137852322
SNPdbers137852322
MSV3drs137852322
GWAS Ctlgrs137852322
Max Magnitude0
OMIM305900
Desc
Variant0014
Relatedalso
ClinVar
Risk rs137852322(C;C)
Alt rs137852322(C;C)
Reference rs137852322(T;T)
Significance Other
Disease G6PD TOMAH
Variation info
Gene G6PD
CLNDBN G6PD TOMAH
Reversed 1
HGVS NC_000023.10:g.153760916A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011101.1,