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rs397515894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397515894(-;-)
Make rs397515894(-;TT)
ReferenceGRCh38 38.1/141
Chromosome11
Position47343136
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515894
ebirs397515894
HLIrs397515894
Exacrs397515894
Varsomers397515894
Maprs397515894
PheGenIrs397515894
hapmaprs397515894
1000 genomesrs397515894
hgdprs397515894
ensemblrs397515894
gopubmedrs397515894
geneviewrs397515894
scholarrs397515894
googlers397515894
pharmgkbrs397515894
gwascentralrs397515894
openSNPrs397515894
23andMers397515894
23andMe allrs397515894
SNP Nexus

SNPshotrs397515894
SNPdbers397515894
MSV3drs397515894
GWAS Ctlgrs397515894
Max Magnitude0
ClinVar
Risk rs397515894(;)
Alt rs397515894(;)
Reference rs397515894(TT;TT)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47364687_47364688delAA
CLNSRC ClinVar
CLNACC RCV000035379.2, RCV000158344.3, RCV000168331.1,