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rs730880533

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880533(A;T)
Make rs730880533(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47343120
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880533
ebirs730880533
HLIrs730880533
Exacrs730880533
Varsomers730880533
Maprs730880533
PheGenIrs730880533
hapmaprs730880533
1000 genomesrs730880533
hgdprs730880533
ensemblrs730880533
gopubmedrs730880533
geneviewrs730880533
scholarrs730880533
googlers730880533
pharmgkbrs730880533
gwascentralrs730880533
openSNPrs730880533
23andMers730880533
23andMe allrs730880533
SNP Nexus

SNPshotrs730880533
SNPdbers730880533
MSV3drs730880533
GWAS Ctlgrs730880533
Max Magnitude0
ClinVar
Risk rs730880533(T;T)
Alt rs730880533(T;T)
Reference rs730880533(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364671T>A
CLNSRC
CLNACC RCV000158071.1,