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rs397515934

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515934(-;-)
Make rs397515934(-;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47341140
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515934
ebirs397515934
HLIrs397515934
Exacrs397515934
Varsomers397515934
Maprs397515934
PheGenIrs397515934
hapmaprs397515934
1000 genomesrs397515934
hgdprs397515934
ensemblrs397515934
gopubmedrs397515934
geneviewrs397515934
scholarrs397515934
googlers397515934
pharmgkbrs397515934
gwascentralrs397515934
openSNPrs397515934
23andMers397515934
23andMe allrs397515934
SNP Nexus

SNPshotrs397515934
SNPdbers397515934
MSV3drs397515934
GWAS Ctlgrs397515934
Max Magnitude0
ClinVar
Risk rs397515934(;)
Alt rs397515934(;)
Reference rs397515934(T;T)
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.47362691delA
CLNSRC ClinVar
CLNACC RCV000035449.2, RCV000158356.1,