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rs397515997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515997(-;-)
Make rs397515997(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position47333707
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397515997
ebirs397515997
HLIrs397515997
Exacrs397515997
Varsomers397515997
Maprs397515997
PheGenIrs397515997
hapmaprs397515997
1000 genomesrs397515997
hgdprs397515997
ensemblrs397515997
gopubmedrs397515997
geneviewrs397515997
scholarrs397515997
googlers397515997
pharmgkbrs397515997
gwascentralrs397515997
openSNPrs397515997
23andMers397515997
23andMe allrs397515997
SNP Nexus

SNPshotrs397515997
SNPdbers397515997
MSV3drs397515997
GWAS Ctlgrs397515997
Max Magnitude0
ClinVar
Risk rs397515997(;)
Alt rs397515997(;)
Reference rs397515997(C;C)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355258delG
CLNSRC ClinVar
CLNACC RCV000035550.5, RCV000211813.1,