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rs397516042

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516042(C;T)
Make rs397516042(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47332075
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516042
ebirs397516042
HLIrs397516042
Exacrs397516042
Varsomers397516042
Maprs397516042
PheGenIrs397516042
hapmaprs397516042
1000 genomesrs397516042
hgdprs397516042
ensemblrs397516042
gopubmedrs397516042
geneviewrs397516042
scholarrs397516042
googlers397516042
pharmgkbrs397516042
gwascentralrs397516042
openSNPrs397516042
23andMers397516042
23andMe allrs397516042
SNP Nexus

SNPshotrs397516042
SNPdbers397516042
MSV3drs397516042
GWAS Ctlgrs397516042
Max Magnitude0
ClinVar
Risk rs397516042(T;T)
Alt rs397516042(T;T)
Reference rs397516042(C;C)
Significance Other
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353626G>A
CLNSRC ClinVar
CLNACC RCV000158271.2, RCV000208264.2,