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rs730880716

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880716(-;-)
Make rs730880716(-;T)
Make rs730880716(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335154
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880716
ebirs730880716
HLIrs730880716
Exacrs730880716
Varsomers730880716
Maprs730880716
PheGenIrs730880716
hapmaprs730880716
1000 genomesrs730880716
hgdprs730880716
ensemblrs730880716
gopubmedrs730880716
geneviewrs730880716
scholarrs730880716
googlers730880716
pharmgkbrs730880716
gwascentralrs730880716
openSNPrs730880716
23andMers730880716
23andMe allrs730880716
SNP Nexus

SNPshotrs730880716
SNPdbers730880716
MSV3drs730880716
GWAS Ctlgrs730880716
Max Magnitude0
ClinVar
Risk rs730880716(T;T)
Alt rs730880716(T;T)
Reference rs730880716(;)
Significance Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy not provided
Reversed 1
HGVS NC_000011.9:g.47356706dupA
CLNSRC
CLNACC RCV000158480.1, RCV000223746.1,