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

rs730880585

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880585(C;C)
Make rs730880585(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333728
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880585
ebirs730880585
HLIrs730880585
Exacrs730880585
Varsomers730880585
Maprs730880585
PheGenIrs730880585
hapmaprs730880585
1000 genomesrs730880585
hgdprs730880585
ensemblrs730880585
gopubmedrs730880585
geneviewrs730880585
scholarrs730880585
googlers730880585
pharmgkbrs730880585
gwascentralrs730880585
openSNPrs730880585
23andMers730880585
23andMe allrs730880585
SNP Nexus

SNPshotrs730880585
SNPdbers730880585
MSV3drs730880585
GWAS Ctlgrs730880585
Max Magnitude0
ClinVar
Risk rs730880585(C;C)
Alt rs730880585(C;C)
Reference rs730880585(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47355279A>G
CLNSRC
CLNACC RCV000158208.1, RCV000223707.1,