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rs137852333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852333(C;T)
Make rs137852333(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532797
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852333
ebirs137852333
HLIrs137852333
Exacrs137852333
Varsomers137852333
Maprs137852333
PheGenIrs137852333
hapmaprs137852333
1000 genomesrs137852333
hgdprs137852333
ensemblrs137852333
gopubmedrs137852333
geneviewrs137852333
scholarrs137852333
googlers137852333
pharmgkbrs137852333
gwascentralrs137852333
openSNPrs137852333
23andMers137852333
23andMe allrs137852333
SNP Nexus

SNPshotrs137852333
SNPdbers137852333
MSV3drs137852333
GWAS Ctlgrs137852333
Max Magnitude0
OMIM305900
Desc
Variant0036
Relatedalso
ClinVar
Risk rs137852333(T;T)
Alt rs137852333(T;T)
Reference rs137852333(C;C)
Significance Other
Disease G6PD IERAPETRA
Variation info
Gene G6PD
CLNDBN G6PD IERAPETRA
Reversed 1
HGVS NC_000023.10:g.153761012G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011115.1,