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rs137852328

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852328(G;T)
Make rs137852328(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154534125
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852328
ebirs137852328
HLIrs137852328
Exacrs137852328
Varsomers137852328
Maprs137852328
PheGenIrs137852328
hapmaprs137852328
1000 genomesrs137852328
hgdprs137852328
ensemblrs137852328
gopubmedrs137852328
geneviewrs137852328
scholarrs137852328
googlers137852328
pharmgkbrs137852328
gwascentralrs137852328
openSNPrs137852328
23andMers137852328
23andMe allrs137852328
SNP Nexus

SNPshotrs137852328
SNPdbers137852328
MSV3drs137852328
GWAS Ctlgrs137852328
Max Magnitude0
OMIM305900
Desc
Variant0027
Relatedalso
OMIM305900
Desc
Variant0035
Relatedalso
ClinVar
Risk rs137852328(A,T;A,T)
Alt rs137852328(A,T;A,T)
Reference rs137852328(G;G)
Significance Other
Disease Glucose 6 phosphate dehydrogenase deficiency G6PD MEXICO CITY
Variation info
Gene G6PD
CLNDBN Glucose 6 phosphate dehydrogenase deficiency G6PD MEXICO CITY
Reversed 1
HGVS NC_000023.10:g.153762340C>A; NC_000023.10:g.153762340C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011118.4, RCV000011131.1,