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rs397515903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515903(A;A)
Make rs397515903(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47342745
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515903
ebirs397515903
HLIrs397515903
Exacrs397515903
Varsomers397515903
Maprs397515903
PheGenIrs397515903
hapmaprs397515903
1000 genomesrs397515903
hgdprs397515903
ensemblrs397515903
gopubmedrs397515903
geneviewrs397515903
scholarrs397515903
googlers397515903
pharmgkbrs397515903
gwascentralrs397515903
openSNPrs397515903
23andMers397515903
23andMe allrs397515903
SNP Nexus

SNPshotrs397515903
SNPdbers397515903
MSV3drs397515903
GWAS Ctlgrs397515903
Max Magnitude0
ClinVar
Risk rs397515903(A;A)
Alt rs397515903(A;A)
Reference rs397515903(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.47364296C>T
CLNSRC ClinVar
CLNACC RCV000035398.3, RCV000158090.2,