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rs730880698

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880698(C;G)
Make rs730880698(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351294
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880698
ebirs730880698
HLIrs730880698
Exacrs730880698
Varsomers730880698
Maprs730880698
PheGenIrs730880698
hapmaprs730880698
1000 genomesrs730880698
hgdprs730880698
ensemblrs730880698
gopubmedrs730880698
geneviewrs730880698
scholarrs730880698
googlers730880698
pharmgkbrs730880698
gwascentralrs730880698
openSNPrs730880698
23andMers730880698
23andMe allrs730880698
SNP Nexus

SNPshotrs730880698
SNPdbers730880698
MSV3drs730880698
GWAS Ctlgrs730880698
Max Magnitude0
ClinVar
Risk rs730880698(G,T;G,T)
Alt rs730880698(G,T;G,T)
Reference rs730880698(C;C)
Significance Pathogenic
Disease not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47372845G>C
CLNSRC
CLNACC RCV000158452.2, RCV000219427.1,