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rs730880614

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880614(C;C)
Make rs730880614(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350101
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880614
ebirs730880614
HLIrs730880614
Exacrs730880614
Varsomers730880614
Maprs730880614
PheGenIrs730880614
hapmaprs730880614
1000 genomesrs730880614
hgdprs730880614
ensemblrs730880614
gopubmedrs730880614
geneviewrs730880614
scholarrs730880614
googlers730880614
pharmgkbrs730880614
gwascentralrs730880614
openSNPrs730880614
23andMers730880614
23andMe allrs730880614
SNP Nexus

SNPshotrs730880614
SNPdbers730880614
MSV3drs730880614
GWAS Ctlgrs730880614
Max Magnitude0
ClinVar
Risk rs730880614(C;C)
Alt rs730880614(C;C)
Reference rs730880614(G;G)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47371652C>G
CLNSRC
CLNACC RCV000158278.1,