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rs397515932

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515932(C;T)
Make rs397515932(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341166
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515932
ebirs397515932
HLIrs397515932
Exacrs397515932
Varsomers397515932
Maprs397515932
PheGenIrs397515932
hapmaprs397515932
1000 genomesrs397515932
hgdprs397515932
ensemblrs397515932
gopubmedrs397515932
geneviewrs397515932
scholarrs397515932
googlers397515932
pharmgkbrs397515932
gwascentralrs397515932
openSNPrs397515932
23andMers397515932
23andMe allrs397515932
SNP Nexus

SNPshotrs397515932
SNPdbers397515932
MSV3drs397515932
GWAS Ctlgrs397515932
Max Magnitude0
ClinVar
Risk rs397515932(A,T;A,T)
Alt rs397515932(A,T;A,T)
Reference rs397515932(C;C)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47362717G>A; NC_000011.9:g.47362717G>T
CLNSRC
CLNACC RCV000035447.2, RCV000151111.2,