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rs137852314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852314(A;A)
Make rs137852314(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154534495
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852314
ebirs137852314
HLIrs137852314
Exacrs137852314
Varsomers137852314
Maprs137852314
PheGenIrs137852314
hapmaprs137852314
1000 genomesrs137852314
hgdprs137852314
ensemblrs137852314
gopubmedrs137852314
geneviewrs137852314
scholarrs137852314
googlers137852314
pharmgkbrs137852314
gwascentralrs137852314
openSNPrs137852314
23andMers137852314
23andMe allrs137852314
SNP Nexus

SNPshotrs137852314
SNPdbers137852314
MSV3drs137852314
GWAS Ctlgrs137852314
Max Magnitude0
OMIM305900
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137852314(A;A)
Alt rs137852314(A;A)
Reference rs137852314(G;G)
Significance Other
Disease G6PD MAHIDOL
Variation info
Gene G6PD
CLNDBN G6PD MAHIDOL
Reversed 1
HGVS NC_000023.10:g.153762710C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011085.2,