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rs397516061

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516061(C;T)
Make rs397516061(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47349815
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516061
ebirs397516061
HLIrs397516061
Exacrs397516061
Varsomers397516061
Maprs397516061
PheGenIrs397516061
hapmaprs397516061
1000 genomesrs397516061
hgdprs397516061
ensemblrs397516061
gopubmedrs397516061
geneviewrs397516061
scholarrs397516061
googlers397516061
pharmgkbrs397516061
gwascentralrs397516061
openSNPrs397516061
23andMers397516061
23andMe allrs397516061
SNP Nexus

SNPshotrs397516061
SNPdbers397516061
MSV3drs397516061
GWAS Ctlgrs397516061
Max Magnitude0
ClinVar
Risk rs397516061(T;T)
Alt rs397516061(T;T)
Reference rs397516061(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47371366G>A
CLNSRC ClinVar
CLNACC RCV000035650.2, RCV000158466.2,