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rs121908987

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908987(A;A)
Make rs121908987(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position151576412
GenePRKAG2
is asnp
is mentioned by
dbSNPrs121908987
ebirs121908987
HLIrs121908987
Exacrs121908987
Varsomers121908987
Maprs121908987
PheGenIrs121908987
hapmaprs121908987
1000 genomesrs121908987
hgdprs121908987
ensemblrs121908987
gopubmedrs121908987
geneviewrs121908987
scholarrs121908987
googlers121908987
pharmgkbrs121908987
gwascentralrs121908987
openSNPrs121908987
23andMers121908987
23andMe allrs121908987
SNP Nexus

SNPshotrs121908987
SNPdbers121908987
MSV3drs121908987
GWAS Ctlgrs121908987
Max Magnitude0
OMIM602743
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908987(A,T;A,T)
Alt rs121908987(A,T;A,T)
Reference rs121908987(G;G)
Significance Pathogenic
Disease Wolff-Parkinson-White pattern Familial hypertrophic cardiomyopathy 6 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene PRKAG2
CLNDBN Wolff-Parkinson-White pattern Familial hypertrophic cardiomyopathy 6 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000007.13:g.151273498C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007248.3, RCV000007249.7, RCV000159005.1, RCV000211845.1,