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

rs730880702

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880702(C;C)
Make rs730880702(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332173
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880702
ebirs730880702
HLIrs730880702
Exacrs730880702
Varsomers730880702
Maprs730880702
PheGenIrs730880702
hapmaprs730880702
1000 genomesrs730880702
hgdprs730880702
ensemblrs730880702
gopubmedrs730880702
geneviewrs730880702
scholarrs730880702
googlers730880702
pharmgkbrs730880702
gwascentralrs730880702
openSNPrs730880702
23andMers730880702
23andMe allrs730880702
SNP Nexus

SNPshotrs730880702
SNPdbers730880702
MSV3drs730880702
GWAS Ctlgrs730880702
Max Magnitude0
ClinVar
Risk rs730880702(C;C)
Alt rs730880702(C;C)
Reference rs730880702(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47353724A>G
CLNSRC
CLNACC RCV000158461.1,