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

rs730880660

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880660(-;-)
Make rs730880660(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47335208
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880660
ebirs730880660
HLIrs730880660
Exacrs730880660
Varsomers730880660
Maprs730880660
PheGenIrs730880660
hapmaprs730880660
1000 genomesrs730880660
hgdprs730880660
ensemblrs730880660
gopubmedrs730880660
geneviewrs730880660
scholarrs730880660
googlers730880660
pharmgkbrs730880660
gwascentralrs730880660
openSNPrs730880660
23andMers730880660
23andMe allrs730880660
SNP Nexus

SNPshotrs730880660
SNPdbers730880660
MSV3drs730880660
GWAS Ctlgrs730880660
Max Magnitude0
ClinVar
Risk rs730880660(;)
Alt rs730880660(;)
Reference rs730880660(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47356759delG
CLNSRC
CLNACC RCV000158377.2,