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rs730880565

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880565(C;T)
Make rs730880565(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337722
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880565
ebirs730880565
HLIrs730880565
Exacrs730880565
Varsomers730880565
Maprs730880565
PheGenIrs730880565
hapmaprs730880565
1000 genomesrs730880565
hgdprs730880565
ensemblrs730880565
gopubmedrs730880565
geneviewrs730880565
scholarrs730880565
googlers730880565
pharmgkbrs730880565
gwascentralrs730880565
openSNPrs730880565
23andMers730880565
23andMe allrs730880565
SNP Nexus

SNPshotrs730880565
SNPdbers730880565
MSV3drs730880565
GWAS Ctlgrs730880565
Max Magnitude0
ClinVar
Risk rs730880565(T;T)
Alt rs730880565(T;T)
Reference rs730880565(C;C)
Significance Probable-Pathogenic
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47359273G>A
CLNSRC
CLNACC RCV000158155.1, RCV000208362.1,