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rs397516039

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516039(C;C)
Make rs397516039(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332133
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs397516039
ebirs397516039
HLIrs397516039
Exacrs397516039
Varsomers397516039
Maprs397516039
PheGenIrs397516039
hapmaprs397516039
1000 genomesrs397516039
hgdprs397516039
ensemblrs397516039
gopubmedrs397516039
geneviewrs397516039
scholarrs397516039
googlers397516039
pharmgkbrs397516039
gwascentralrs397516039
openSNPrs397516039
23andMers397516039
23andMe allrs397516039
SNP Nexus

SNPshotrs397516039
SNPdbers397516039
MSV3drs397516039
GWAS Ctlgrs397516039
Max Magnitude0
ClinVar
Risk rs397516039(C,G;C,G)
Alt rs397516039(C,G;C,G)
Reference rs397516039(T;T)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000011.9:g.47353684A>C; NC_000011.9:g.47353684A>G
CLNSRC
CLNACC RCV000154451.2, RCV000035615.2,