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

rs730880649

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880649(-;-)
Make rs730880649(-;A)
Make rs730880649(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341196
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880649
ebirs730880649
HLIrs730880649
Exacrs730880649
Varsomers730880649
Maprs730880649
PheGenIrs730880649
hapmaprs730880649
1000 genomesrs730880649
hgdprs730880649
ensemblrs730880649
gopubmedrs730880649
geneviewrs730880649
scholarrs730880649
googlers730880649
pharmgkbrs730880649
gwascentralrs730880649
openSNPrs730880649
23andMers730880649
23andMe allrs730880649
SNP Nexus

SNPshotrs730880649
SNPdbers730880649
MSV3drs730880649
GWAS Ctlgrs730880649
Max Magnitude0
ClinVar
Risk rs730880649(A;A)
Alt rs730880649(A;A)
Reference rs730880649(;)
Significance Pathogenic
Disease Cardiomyopathy Familial hypertrophic cardiomyopathy 1 not provided
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy Familial hypertrophic cardiomyopathy 1 not provided
Reversed 1
HGVS NC_000011.9:g.47362748dupT
CLNSRC
CLNACC RCV000158355.1, RCV000201914.1, RCV000223830.1,