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rs397515935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515935(A;A)
Make rs397515935(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47341137
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515935
ebirs397515935
HLIrs397515935
Exacrs397515935
Varsomers397515935
Maprs397515935
PheGenIrs397515935
hapmaprs397515935
1000 genomesrs397515935
hgdprs397515935
ensemblrs397515935
gopubmedrs397515935
geneviewrs397515935
scholarrs397515935
googlers397515935
pharmgkbrs397515935
gwascentralrs397515935
openSNPrs397515935
23andMers397515935
23andMe allrs397515935
SNP Nexus

SNPshotrs397515935
SNPdbers397515935
MSV3drs397515935
GWAS Ctlgrs397515935
Max Magnitude0
ClinVar
Risk rs397515935(A;A)
Alt rs397515935(A;A)
Reference rs397515935(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.47362688C>T
CLNSRC ClinVar
CLNACC RCV000035450.3, RCV000158128.1,