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

rs730880651

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880651(-;-)
Make rs730880651(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47338561
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880651
ebirs730880651
HLIrs730880651
Exacrs730880651
Varsomers730880651
Maprs730880651
PheGenIrs730880651
hapmaprs730880651
1000 genomesrs730880651
hgdprs730880651
ensemblrs730880651
gopubmedrs730880651
geneviewrs730880651
scholarrs730880651
googlers730880651
pharmgkbrs730880651
gwascentralrs730880651
openSNPrs730880651
23andMers730880651
23andMe allrs730880651
SNP Nexus

SNPshotrs730880651
SNPdbers730880651
MSV3drs730880651
GWAS Ctlgrs730880651
Max Magnitude0
ClinVar
Risk rs730880651(;)
Alt rs730880651(;)
Reference rs730880651(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47360112delG
CLNSRC
CLNACC RCV000158360.1,