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rs137852348

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852348(C;G)
Make rs137852348(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532203
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852348
ebirs137852348
HLIrs137852348
Exacrs137852348
Varsomers137852348
Maprs137852348
PheGenIrs137852348
hapmaprs137852348
1000 genomesrs137852348
hgdprs137852348
ensemblrs137852348
gopubmedrs137852348
geneviewrs137852348
scholarrs137852348
googlers137852348
pharmgkbrs137852348
gwascentralrs137852348
openSNPrs137852348
23andMers137852348
23andMe allrs137852348
SNP Nexus

SNPshotrs137852348
SNPdbers137852348
MSV3drs137852348
GWAS Ctlgrs137852348
Max Magnitude0
OMIM305900
Desc
Variant0060
Relatedalso
ClinVar
Risk rs137852348(G;G)
Alt rs137852348(G;G)
Reference rs137852348(C;C)
Significance Other
Disease G6PD SPLIT
Variation info
Gene G6PD
CLNDBN G6PD SPLIT
Reversed 1
HGVS NC_000023.10:g.153760418G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011159.3,