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rs397516067

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516067(A;A)
Make rs397516067(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47348542
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516067
ebirs397516067
HLIrs397516067
Exacrs397516067
Varsomers397516067
Maprs397516067
PheGenIrs397516067
hapmaprs397516067
1000 genomesrs397516067
hgdprs397516067
ensemblrs397516067
gopubmedrs397516067
geneviewrs397516067
scholarrs397516067
googlers397516067
pharmgkbrs397516067
gwascentralrs397516067
openSNPrs397516067
23andMers397516067
23andMe allrs397516067
SNP Nexus

SNPshotrs397516067
SNPdbers397516067
MSV3drs397516067
GWAS Ctlgrs397516067
Max Magnitude0
ClinVar
Risk rs397516067(A;A)
Alt rs397516067(A;A)
Reference rs397516067(G;G)
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.47370093C>T
CLNSRC ClinVar
CLNACC RCV000035659.2, RCV000158302.2,