Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880621

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880621(G;T)
Make rs730880621(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349773
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880621
ebirs730880621
HLIrs730880621
Exacrs730880621
Varsomers730880621
Maprs730880621
PheGenIrs730880621
hapmaprs730880621
1000 genomesrs730880621
hgdprs730880621
ensemblrs730880621
gopubmedrs730880621
geneviewrs730880621
scholarrs730880621
googlers730880621
pharmgkbrs730880621
gwascentralrs730880621
openSNPrs730880621
23andMers730880621
23andMe allrs730880621
SNP Nexus

SNPshotrs730880621
SNPdbers730880621
MSV3drs730880621
GWAS Ctlgrs730880621
Max Magnitude0
ClinVar
Risk rs730880621(A,T;A,T)
Alt rs730880621(A,T;A,T)
Reference rs730880621(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371324C>A
CLNSRC
CLNACC RCV000158289.1,