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rs730880594

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880594(C;T)
Make rs730880594(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332612
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880594
ebirs730880594
HLIrs730880594
Exacrs730880594
Varsomers730880594
Maprs730880594
PheGenIrs730880594
hapmaprs730880594
1000 genomesrs730880594
hgdprs730880594
ensemblrs730880594
gopubmedrs730880594
geneviewrs730880594
scholarrs730880594
googlers730880594
pharmgkbrs730880594
gwascentralrs730880594
openSNPrs730880594
23andMers730880594
23andMe allrs730880594
SNP Nexus

SNPshotrs730880594
SNPdbers730880594
MSV3drs730880594
GWAS Ctlgrs730880594
Max Magnitude0
ClinVar
Risk rs730880594(T;T)
Alt rs730880594(T;T)
Reference rs730880594(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYBPC3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000011.9:g.47354163G>A
CLNSRC
CLNACC RCV000158244.1, RCV000223738.1,