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

rs730880605

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880605(C;T)
Make rs730880605(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332111
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880605
ebirs730880605
HLIrs730880605
Exacrs730880605
Varsomers730880605
Maprs730880605
PheGenIrs730880605
hapmaprs730880605
1000 genomesrs730880605
hgdprs730880605
ensemblrs730880605
gopubmedrs730880605
geneviewrs730880605
scholarrs730880605
googlers730880605
pharmgkbrs730880605
gwascentralrs730880605
openSNPrs730880605
23andMers730880605
23andMe allrs730880605
SNP Nexus

SNPshotrs730880605
SNPdbers730880605
MSV3drs730880605
GWAS Ctlgrs730880605
Max Magnitude0
ClinVar
Risk rs730880605(T;T)
Alt rs730880605(T;T)
Reference rs730880605(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47353662G>A
CLNSRC
CLNACC RCV000158263.1,