Have questions? Visit https://www.reddit.com/r/SNPedia

rs730880564

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880564(C;G)
Make rs730880564(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337779
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880564
ebirs730880564
HLIrs730880564
Exacrs730880564
Varsomers730880564
Maprs730880564
PheGenIrs730880564
hapmaprs730880564
1000 genomesrs730880564
hgdprs730880564
ensemblrs730880564
gopubmedrs730880564
geneviewrs730880564
scholarrs730880564
googlers730880564
pharmgkbrs730880564
gwascentralrs730880564
openSNPrs730880564
23andMers730880564
23andMe allrs730880564
SNP Nexus

SNPshotrs730880564
SNPdbers730880564
MSV3drs730880564
GWAS Ctlgrs730880564
Max Magnitude0
ClinVar
Risk rs730880564(G;G)
Alt rs730880564(G;G)
Reference rs730880564(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359330G>C
CLNSRC
CLNACC RCV000158153.1,