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rs137852313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852313(A;A)
Make rs137852313(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154535187
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852313
ebirs137852313
HLIrs137852313
Exacrs137852313
Varsomers137852313
Maprs137852313
PheGenIrs137852313
hapmaprs137852313
1000 genomesrs137852313
hgdprs137852313
ensemblrs137852313
gopubmedrs137852313
geneviewrs137852313
scholarrs137852313
googlers137852313
pharmgkbrs137852313
gwascentralrs137852313
openSNPrs137852313
23andMers137852313
23andMe allrs137852313
SNP Nexus

SNPshotrs137852313
SNPdbers137852313
MSV3drs137852313
GWAS Ctlgrs137852313
GMAF0.0
Max Magnitude0
OMIM305900
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852313(A;A)
Alt rs137852313(A;A)
Reference rs137852313(G;G)
Significance Other
Disease G6PD ILESHA
Variation info
Gene G6PD
CLNDBN G6PD ILESHA
Reversed 1
HGVS NC_000023.10:g.153763402C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011082.4,