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rs730880666

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880666(AA;AA)
Make rs730880666(AA;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333668
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880666
ebirs730880666
HLIrs730880666
Exacrs730880666
Varsomers730880666
Maprs730880666
PheGenIrs730880666
hapmaprs730880666
1000 genomesrs730880666
hgdprs730880666
ensemblrs730880666
gopubmedrs730880666
geneviewrs730880666
scholarrs730880666
googlers730880666
pharmgkbrs730880666
gwascentralrs730880666
openSNPrs730880666
23andMers730880666
23andMe allrs730880666
SNP Nexus

SNPshotrs730880666
SNPdbers730880666
MSV3drs730880666
GWAS Ctlgrs730880666
Max Magnitude0
ClinVar
Risk rs730880666(AA;AA)
Alt rs730880666(AA;AA)
Reference rs730880666(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355219delCinsTT
CLNSRC
CLNACC RCV000158389.1,