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rs397515979

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515979(-;-)
Make rs397515979(-;C)
Make rs397515979(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position47336003
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515979
ebirs397515979
HLIrs397515979
Exacrs397515979
Varsomers397515979
Maprs397515979
PheGenIrs397515979
hapmaprs397515979
1000 genomesrs397515979
hgdprs397515979
ensemblrs397515979
gopubmedrs397515979
geneviewrs397515979
scholarrs397515979
googlers397515979
pharmgkbrs397515979
gwascentralrs397515979
openSNPrs397515979
23andMers397515979
23andMe allrs397515979
SNP Nexus

SNPshotrs397515979
SNPdbers397515979
MSV3drs397515979
GWAS Ctlgrs397515979
Max Magnitude0
ClinVar
Risk rs397515979(C;C)
Alt rs397515979(C;C)
Reference rs397515979(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47357555dupG
CLNSRC ClinVar
CLNACC RCV000035514.2, RCV000158373.1,