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rs137852324

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852324(A;A)
Make rs137852324(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532389
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852324
ebirs137852324
HLIrs137852324
Exacrs137852324
Varsomers137852324
Maprs137852324
PheGenIrs137852324
hapmaprs137852324
1000 genomesrs137852324
hgdprs137852324
ensemblrs137852324
gopubmedrs137852324
geneviewrs137852324
scholarrs137852324
googlers137852324
pharmgkbrs137852324
gwascentralrs137852324
openSNPrs137852324
23andMers137852324
23andMe allrs137852324
SNP Nexus

SNPshotrs137852324
SNPdbers137852324
MSV3drs137852324
GWAS Ctlgrs137852324
Max Magnitude0
OMIM305900
Desc
Variant0020
Relatedalso
ClinVar
Risk rs137852324(A;A)
Alt rs137852324(A;A)
Reference rs137852324(G;G)
Significance Other
Disease G6PD ANDALUS
Variation info
Gene G6PD
CLNDBN G6PD ANDALUS
Reversed 1
HGVS NC_000023.10:g.153760604C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011103.1,