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

rs730880622

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880622(C;C)
Make rs730880622(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47349857
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880622
ebirs730880622
HLIrs730880622
Exacrs730880622
Varsomers730880622
Maprs730880622
PheGenIrs730880622
hapmaprs730880622
1000 genomesrs730880622
hgdprs730880622
ensemblrs730880622
gopubmedrs730880622
geneviewrs730880622
scholarrs730880622
googlers730880622
pharmgkbrs730880622
gwascentralrs730880622
openSNPrs730880622
23andMers730880622
23andMe allrs730880622
SNP Nexus

SNPshotrs730880622
SNPdbers730880622
MSV3drs730880622
GWAS Ctlgrs730880622
Max Magnitude0
ClinVar
Risk rs730880622(C;C)
Alt rs730880622(C;C)
Reference rs730880622(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47371408A>G
CLNSRC
CLNACC RCV000158296.1,