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

rs730880541

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880541(C;T)
Make rs730880541(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342840
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880541
ebirs730880541
HLIrs730880541
Exacrs730880541
Varsomers730880541
Maprs730880541
PheGenIrs730880541
hapmaprs730880541
1000 genomesrs730880541
hgdprs730880541
ensemblrs730880541
gopubmedrs730880541
geneviewrs730880541
scholarrs730880541
googlers730880541
pharmgkbrs730880541
gwascentralrs730880541
openSNPrs730880541
23andMers730880541
23andMe allrs730880541
SNP Nexus

SNPshotrs730880541
SNPdbers730880541
MSV3drs730880541
GWAS Ctlgrs730880541
Max Magnitude0
ClinVar
Risk rs730880541(T;T)
Alt rs730880541(T;T)
Reference rs730880541(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364391G>A
CLNSRC
CLNACC RCV000158085.2,