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rs730880578

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880578(C;T)
Make rs730880578(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335054
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880578
ebirs730880578
HLIrs730880578
Exacrs730880578
Varsomers730880578
Maprs730880578
PheGenIrs730880578
hapmaprs730880578
1000 genomesrs730880578
hgdprs730880578
ensemblrs730880578
gopubmedrs730880578
geneviewrs730880578
scholarrs730880578
googlers730880578
pharmgkbrs730880578
gwascentralrs730880578
openSNPrs730880578
23andMers730880578
23andMe allrs730880578
SNP Nexus

SNPshotrs730880578
SNPdbers730880578
MSV3drs730880578
GWAS Ctlgrs730880578
Max Magnitude0
ClinVar
Risk rs730880578(T;T)
Alt rs730880578(T;T)
Reference rs730880578(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47356605G>A
CLNSRC
CLNACC RCV000158193.1,