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rs137852321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852321(A;A)
Make rs137852321(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532694
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852321
ebirs137852321
HLIrs137852321
Exacrs137852321
Varsomers137852321
Maprs137852321
PheGenIrs137852321
hapmaprs137852321
1000 genomesrs137852321
hgdprs137852321
ensemblrs137852321
gopubmedrs137852321
geneviewrs137852321
scholarrs137852321
googlers137852321
pharmgkbrs137852321
gwascentralrs137852321
openSNPrs137852321
23andMers137852321
23andMe allrs137852321
SNP Nexus

SNPshotrs137852321
SNPdbers137852321
MSV3drs137852321
GWAS Ctlgrs137852321
Max Magnitude0
OMIM305900
Desc
Variant0013
Relatedalso
ClinVar
Risk rs137852321(A;A)
Alt rs137852321(A;A)
Reference rs137852321(G;G)
Significance Other
Disease G6PD BEVERLY HILLS
Variation info
Gene G6PD
CLNDBN G6PD BEVERLY HILLS
Reversed 1
HGVS NC_000023.10:g.153760909C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011100.1,