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rs397515902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515902(G;G)
Make rs397515902(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47342831
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515902
ebirs397515902
HLIrs397515902
Exacrs397515902
Varsomers397515902
Maprs397515902
PheGenIrs397515902
hapmaprs397515902
1000 genomesrs397515902
hgdprs397515902
ensemblrs397515902
gopubmedrs397515902
geneviewrs397515902
scholarrs397515902
googlers397515902
pharmgkbrs397515902
gwascentralrs397515902
openSNPrs397515902
23andMers397515902
23andMe allrs397515902
SNP Nexus

SNPshotrs397515902
SNPdbers397515902
MSV3drs397515902
GWAS Ctlgrs397515902
Max Magnitude0
ClinVar
Risk rs397515902(C,G;C,G)
Alt rs397515902(C,G;C,G)
Reference rs397515902(T;T)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified not provided
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified not provided
Reversed 1
HGVS NC_000011.9:g.47364382A>C; NC_000011.9:g.47364382A>G
CLNSRC ClinVar
CLNACC RCV000035397.2, RCV000168775.1, RCV000174994.1,