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rs137852344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852344(C;G)
Make rs137852344(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532245
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852344
ebirs137852344
HLIrs137852344
Exacrs137852344
Varsomers137852344
Maprs137852344
PheGenIrs137852344
hapmaprs137852344
1000 genomesrs137852344
hgdprs137852344
ensemblrs137852344
gopubmedrs137852344
geneviewrs137852344
scholarrs137852344
googlers137852344
pharmgkbrs137852344
gwascentralrs137852344
openSNPrs137852344
23andMers137852344
23andMe allrs137852344
SNP Nexus

SNPshotrs137852344
SNPdbers137852344
MSV3drs137852344
GWAS Ctlgrs137852344
Max Magnitude0
OMIM305900
Desc
Variant0050
Relatedalso
ClinVar
Risk rs137852344(G;G)
Alt rs137852344(G;G)
Reference rs137852344(C;C)
Significance Other
Disease G6PD NEAPOLIS
Variation info
Gene G6PD
CLNDBN G6PD NEAPOLIS
Reversed 1
HGVS NC_000023.10:g.153760460G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011152.2,