Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852323(G;T)
Make rs137852323(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532626
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852323
ebirs137852323
HLIrs137852323
Exacrs137852323
Varsomers137852323
Maprs137852323
PheGenIrs137852323
hapmaprs137852323
1000 genomesrs137852323
hgdprs137852323
ensemblrs137852323
gopubmedrs137852323
geneviewrs137852323
scholarrs137852323
googlers137852323
pharmgkbrs137852323
gwascentralrs137852323
openSNPrs137852323
23andMers137852323
23andMe allrs137852323
SNP Nexus

SNPshotrs137852323
SNPdbers137852323
MSV3drs137852323
GWAS Ctlgrs137852323
Max Magnitude0
OMIM305900
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137852323(T;T)
Alt rs137852323(T;T)
Reference rs137852323(G;G)
Significance Other
Disease G6PD RIVERSIDE
Variation info
Gene G6PD
CLNDBN G6PD RIVERSIDE
Reversed 1
HGVS NC_000023.10:g.153760841C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011102.1,