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rs730880581

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880581(A;A)
Make rs730880581(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351296
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880581
ebirs730880581
HLIrs730880581
Exacrs730880581
Varsomers730880581
Maprs730880581
PheGenIrs730880581
hapmaprs730880581
1000 genomesrs730880581
hgdprs730880581
ensemblrs730880581
gopubmedrs730880581
geneviewrs730880581
scholarrs730880581
googlers730880581
pharmgkbrs730880581
gwascentralrs730880581
openSNPrs730880581
23andMers730880581
23andMe allrs730880581
SNP Nexus

SNPshotrs730880581
SNPdbers730880581
MSV3drs730880581
GWAS Ctlgrs730880581
Max Magnitude0
ClinVar
Risk rs730880581(A;A)
Alt rs730880581(A;A)
Reference rs730880581(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372847A>T
CLNSRC
CLNACC RCV000158200.1,