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rs397515897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515897(C;C)
Make rs397515897(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47343019
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515897
ebirs397515897
HLIrs397515897
Exacrs397515897
Varsomers397515897
Maprs397515897
PheGenIrs397515897
hapmaprs397515897
1000 genomesrs397515897
hgdprs397515897
ensemblrs397515897
gopubmedrs397515897
geneviewrs397515897
scholarrs397515897
googlers397515897
pharmgkbrs397515897
gwascentralrs397515897
openSNPrs397515897
23andMers397515897
23andMe allrs397515897
SNP Nexus

SNPshotrs397515897
SNPdbers397515897
MSV3drs397515897
GWAS Ctlgrs397515897
Max Magnitude0
ClinVar
Risk rs397515897(C;C)
Alt rs397515897(C;C)
Reference rs397515897(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.47364570A>G
CLNSRC ClinVar
CLNACC RCV000035391.2, RCV000158072.1,