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rs267606976

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606976(C;C)
Make rs267606976(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position151564203
GenePRKAG2
is asnp
is mentioned by
dbSNPrs267606976
ebirs267606976
HLIrs267606976
Exacrs267606976
Varsomers267606976
Maprs267606976
PheGenIrs267606976
hapmaprs267606976
1000 genomesrs267606976
hgdprs267606976
ensemblrs267606976
gopubmedrs267606976
geneviewrs267606976
scholarrs267606976
googlers267606976
pharmgkbrs267606976
gwascentralrs267606976
openSNPrs267606976
23andMers267606976
23andMe allrs267606976
SNP Nexus

SNPshotrs267606976
SNPdbers267606976
MSV3drs267606976
GWAS Ctlgrs267606976
Max Magnitude0
ClinVar
Risk rs267606976(C;C)
Alt rs267606976(C;C)
Reference rs267606976(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.151261289A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007256.5, RCV000159015.2,