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rs397516032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516032(-;-)
Make rs397516032(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position47350546
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516032
ebirs397516032
HLIrs397516032
Exacrs397516032
Varsomers397516032
Maprs397516032
PheGenIrs397516032
hapmaprs397516032
1000 genomesrs397516032
hgdprs397516032
ensemblrs397516032
gopubmedrs397516032
geneviewrs397516032
scholarrs397516032
googlers397516032
pharmgkbrs397516032
gwascentralrs397516032
openSNPrs397516032
23andMers397516032
23andMe allrs397516032
SNP Nexus

SNPshotrs397516032
SNPdbers397516032
MSV3drs397516032
GWAS Ctlgrs397516032
Max Magnitude0
ClinVar
Risk rs397516032(;)
Alt rs397516032(;)
Reference rs397516032(C;C)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47372097delG
CLNSRC ClinVar
CLNACC RCV000035604.2,