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rs397515960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515960(-;-)
Make rs397515960(-;G)
Make rs397515960(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47337791
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515960
ebirs397515960
HLIrs397515960
Exacrs397515960
Varsomers397515960
Maprs397515960
PheGenIrs397515960
hapmaprs397515960
1000 genomesrs397515960
hgdprs397515960
ensemblrs397515960
gopubmedrs397515960
geneviewrs397515960
scholarrs397515960
googlers397515960
pharmgkbrs397515960
gwascentralrs397515960
openSNPrs397515960
23andMers397515960
23andMe allrs397515960
SNP Nexus

SNPshotrs397515960
SNPdbers397515960
MSV3drs397515960
GWAS Ctlgrs397515960
Max Magnitude0
ClinVar
Risk rs397515960(G;G)
Alt rs397515960(G;G)
Reference rs397515960(;)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47359343dupC
CLNSRC ClinVar
CLNACC RCV000035483.2, RCV000158361.1,