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rs730880604

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880604(G;G)
Make rs730880604(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332113
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880604
ebirs730880604
HLIrs730880604
Exacrs730880604
Varsomers730880604
Maprs730880604
PheGenIrs730880604
hapmaprs730880604
1000 genomesrs730880604
hgdprs730880604
ensemblrs730880604
gopubmedrs730880604
geneviewrs730880604
scholarrs730880604
googlers730880604
pharmgkbrs730880604
gwascentralrs730880604
openSNPrs730880604
23andMers730880604
23andMe allrs730880604
SNP Nexus

SNPshotrs730880604
SNPdbers730880604
MSV3drs730880604
GWAS Ctlgrs730880604
Max Magnitude0
ClinVar
Risk rs730880604(G;G)
Alt rs730880604(G;G)
Reference rs730880604(T;T)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47353664A>C
CLNSRC
CLNACC RCV000158262.1,