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rs137852341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852341(G;T)
Make rs137852341(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154535261
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852341
ebirs137852341
HLIrs137852341
Exacrs137852341
Varsomers137852341
Maprs137852341
PheGenIrs137852341
hapmaprs137852341
1000 genomesrs137852341
hgdprs137852341
ensemblrs137852341
gopubmedrs137852341
geneviewrs137852341
scholarrs137852341
googlers137852341
pharmgkbrs137852341
gwascentralrs137852341
openSNPrs137852341
23andMers137852341
23andMe allrs137852341
SNP Nexus

SNPshotrs137852341
SNPdbers137852341
MSV3drs137852341
GWAS Ctlgrs137852341
GMAF0.0006046
Max Magnitude0
OMIM305900
Desc
Variant0045
Relatedalso
ClinVar
Risk rs137852341(A,T;A,T)
Alt rs137852341(A,T;A,T)
Reference rs137852341(G;G)
Significance Other
Disease G6PD QUING YUAN
Variation info
Gene G6PD
CLNDBN G6PD QUING YUAN
Reversed 1
HGVS NC_000023.10:g.153763476C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011147.1,