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rs267606979

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606979(C;C)
Make rs267606979(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position151560560
GenePRKAG2
is asnp
is mentioned by
dbSNPrs267606979
ebirs267606979
HLIrs267606979
Exacrs267606979
Varsomers267606979
Maprs267606979
PheGenIrs267606979
hapmaprs267606979
1000 genomesrs267606979
hgdprs267606979
ensemblrs267606979
gopubmedrs267606979
geneviewrs267606979
scholarrs267606979
googlers267606979
pharmgkbrs267606979
gwascentralrs267606979
openSNPrs267606979
23andMers267606979
23andMe allrs267606979
SNP Nexus

SNPshotrs267606979
SNPdbers267606979
MSV3drs267606979
GWAS Ctlgrs267606979
Max Magnitude0
ClinVar
Risk rs267606979(C;C)
Alt rs267606979(C;C)
Reference rs267606979(T;T)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 6 not provided
Variation info
Gene PRKAG2
CLNDBN Familial hypertrophic cardiomyopathy 6 not provided
Reversed 1
HGVS NC_000007.13:g.151257646A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007259.2, RCV000159020.1,