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rs267606978

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606978(C;C)
Make rs267606978(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position151564146
GenePRKAG2
is asnp
is mentioned by
dbSNPrs267606978
ebirs267606978
HLIrs267606978
Exacrs267606978
Varsomers267606978
Maprs267606978
PheGenIrs267606978
hapmaprs267606978
1000 genomesrs267606978
hgdprs267606978
ensemblrs267606978
gopubmedrs267606978
geneviewrs267606978
scholarrs267606978
googlers267606978
pharmgkbrs267606978
gwascentralrs267606978
openSNPrs267606978
23andMers267606978
23andMe allrs267606978
SNP Nexus

SNPshotrs267606978
SNPdbers267606978
MSV3drs267606978
GWAS Ctlgrs267606978
Max Magnitude0
ClinVar
Risk rs267606978(C;C)
Alt rs267606978(C;C)
Reference rs267606978(G;G)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 6 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene PRKAG2
CLNDBN Familial hypertrophic cardiomyopathy 6 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000007.13:g.151261232C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007258.6, RCV000159017.1, RCV000211740.1,