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rs397515944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515944(-;-)
Make rs397515944(-;T)
Make rs397515944(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47339677
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515944
ebirs397515944
HLIrs397515944
Exacrs397515944
Varsomers397515944
Maprs397515944
PheGenIrs397515944
hapmaprs397515944
1000 genomesrs397515944
hgdprs397515944
ensemblrs397515944
gopubmedrs397515944
geneviewrs397515944
scholarrs397515944
googlers397515944
pharmgkbrs397515944
gwascentralrs397515944
openSNPrs397515944
23andMers397515944
23andMe allrs397515944
SNP Nexus

SNPshotrs397515944
SNPdbers397515944
MSV3drs397515944
GWAS Ctlgrs397515944
Max Magnitude0
ClinVar
Risk rs397515944(T;T)
Alt rs397515944(T;T)
Reference rs397515944(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47361229dupA
CLNSRC ClinVar
CLNACC RCV000035461.2,