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rs730880561

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880561(C;T)
Make rs730880561(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47339716
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880561
ebirs730880561
HLIrs730880561
Exacrs730880561
Varsomers730880561
Maprs730880561
PheGenIrs730880561
hapmaprs730880561
1000 genomesrs730880561
hgdprs730880561
ensemblrs730880561
gopubmedrs730880561
geneviewrs730880561
scholarrs730880561
googlers730880561
pharmgkbrs730880561
gwascentralrs730880561
openSNPrs730880561
23andMers730880561
23andMe allrs730880561
SNP Nexus

SNPshotrs730880561
SNPdbers730880561
MSV3drs730880561
GWAS Ctlgrs730880561
Max Magnitude0
ClinVar
Risk rs730880561(T;T)
Alt rs730880561(T;T)
Reference rs730880561(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47361267G>A
CLNSRC
CLNACC RCV000158136.1,