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rs137852530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852530(A;A)
Make rs137852530(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position78124992
GenePGK1
is asnp
is mentioned by
dbSNPrs137852530
ebirs137852530
HLIrs137852530
Exacrs137852530
Varsomers137852530
Maprs137852530
PheGenIrs137852530
hapmaprs137852530
1000 genomesrs137852530
hgdprs137852530
ensemblrs137852530
gopubmedrs137852530
geneviewrs137852530
scholarrs137852530
googlers137852530
pharmgkbrs137852530
gwascentralrs137852530
openSNPrs137852530
23andMers137852530
23andMe allrs137852530
SNP Nexus

SNPshotrs137852530
SNPdbers137852530
MSV3drs137852530
GWAS Ctlgrs137852530
Max Magnitude0
OMIM311800
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137852530(A;A)
Alt rs137852530(A;A)
Reference rs137852530(C;C)
Significance Other
Disease Phosphoglycerate kinase electrophoretic variant PGK II
Variation info
Gene PGK1
CLNDBN Phosphoglycerate kinase electrophoretic variant PGK II
Reversed 0
HGVS NC_000023.10:g.77380489C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010623.2,