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rs730880655

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880655(-;-)
Make rs730880655(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47336010
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880655
ebirs730880655
HLIrs730880655
Exacrs730880655
Varsomers730880655
Maprs730880655
PheGenIrs730880655
hapmaprs730880655
1000 genomesrs730880655
hgdprs730880655
ensemblrs730880655
gopubmedrs730880655
geneviewrs730880655
scholarrs730880655
googlers730880655
pharmgkbrs730880655
gwascentralrs730880655
openSNPrs730880655
23andMers730880655
23andMe allrs730880655
SNP Nexus

SNPshotrs730880655
SNPdbers730880655
MSV3drs730880655
GWAS Ctlgrs730880655
Max Magnitude0
ClinVar
Risk rs730880655(;)
Alt rs730880655(;)
Reference rs730880655(T;T)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47357561delA
CLNSRC
CLNACC RCV000158371.1,