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rs730880648

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880648(-;-)
Make rs730880648(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341229
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880648
ebirs730880648
HLIrs730880648
Exacrs730880648
Varsomers730880648
Maprs730880648
PheGenIrs730880648
hapmaprs730880648
1000 genomesrs730880648
hgdprs730880648
ensemblrs730880648
gopubmedrs730880648
geneviewrs730880648
scholarrs730880648
googlers730880648
pharmgkbrs730880648
gwascentralrs730880648
openSNPrs730880648
23andMers730880648
23andMe allrs730880648
SNP Nexus

SNPshotrs730880648
SNPdbers730880648
MSV3drs730880648
GWAS Ctlgrs730880648
Max Magnitude0
ClinVar
Risk rs730880648(;)
Alt rs730880648(;)
Reference rs730880648(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47362780delG
CLNSRC
CLNACC RCV000158354.1,