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rs730880554

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880554(A;T)
Make rs730880554(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341206
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880554
ebirs730880554
HLIrs730880554
Exacrs730880554
Varsomers730880554
Maprs730880554
PheGenIrs730880554
hapmaprs730880554
1000 genomesrs730880554
hgdprs730880554
ensemblrs730880554
gopubmedrs730880554
geneviewrs730880554
scholarrs730880554
googlers730880554
pharmgkbrs730880554
gwascentralrs730880554
openSNPrs730880554
23andMers730880554
23andMe allrs730880554
SNP Nexus

SNPshotrs730880554
SNPdbers730880554
MSV3drs730880554
GWAS Ctlgrs730880554
Max Magnitude0
ClinVar
Risk rs730880554(T;T)
Alt rs730880554(T;T)
Reference rs730880554(A;A)
Significance Pathogenic
Disease not provided Hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not provided Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47362757T>A
CLNSRC
CLNACC RCV000158124.1, RCV000233359.1,