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rs137852349

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852349(C;C)
Make rs137852349(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154535996
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852349
ebirs137852349
HLIrs137852349
Exacrs137852349
Varsomers137852349
Maprs137852349
PheGenIrs137852349
hapmaprs137852349
1000 genomesrs137852349
hgdprs137852349
ensemblrs137852349
gopubmedrs137852349
geneviewrs137852349
scholarrs137852349
googlers137852349
pharmgkbrs137852349
gwascentralrs137852349
openSNPrs137852349
23andMers137852349
23andMe allrs137852349
SNP Nexus

SNPshotrs137852349
SNPdbers137852349
MSV3drs137852349
GWAS Ctlgrs137852349
Max Magnitude0
OMIM305900
Desc
Variant0061
Relatedalso
ClinVar
Risk rs137852349(C;C)
Alt rs137852349(C;C)
Reference rs137852349(T;T)
Significance Other
Disease G6PD NAMORU
Variation info
Gene G6PD
CLNDBN G6PD NAMORU
Reversed 1
HGVS NC_000023.10:g.153764211A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000011160.3,