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rs730880588

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880588(C;C)
Make rs730880588(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333658
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880588
ebirs730880588
HLIrs730880588
Exacrs730880588
Varsomers730880588
Maprs730880588
PheGenIrs730880588
hapmaprs730880588
1000 genomesrs730880588
hgdprs730880588
ensemblrs730880588
gopubmedrs730880588
geneviewrs730880588
scholarrs730880588
googlers730880588
pharmgkbrs730880588
gwascentralrs730880588
openSNPrs730880588
23andMers730880588
23andMe allrs730880588
SNP Nexus

SNPshotrs730880588
SNPdbers730880588
MSV3drs730880588
GWAS Ctlgrs730880588
Max Magnitude0
ClinVar
Risk rs730880588(C;C)
Alt rs730880588(C;C)
Reference Rs730880588(T;T)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47355209A>G
CLNSRC
CLNACC RCV000158214.1,