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rs730880630

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880630(C;T)
Make rs730880630(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346294
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880630
ebirs730880630
HLIrs730880630
Exacrs730880630
Varsomers730880630
Maprs730880630
PheGenIrs730880630
hapmaprs730880630
1000 genomesrs730880630
hgdprs730880630
ensemblrs730880630
gopubmedrs730880630
geneviewrs730880630
scholarrs730880630
googlers730880630
pharmgkbrs730880630
gwascentralrs730880630
openSNPrs730880630
23andMers730880630
23andMe allrs730880630
SNP Nexus

SNPshotrs730880630
SNPdbers730880630
MSV3drs730880630
GWAS Ctlgrs730880630
Max Magnitude0
ClinVar
Risk rs730880630(T;T)
Alt rs730880630(T;T)
Reference rs730880630(C;C)
Significance Probable-Pathogenic
Disease not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47367845G>A
CLNSRC
CLNACC RCV000158326.1, RCV000200384.1,