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rs730880566

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880566(A;A)
Make rs730880566(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337579
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880566
ebirs730880566
HLIrs730880566
Exacrs730880566
Varsomers730880566
Maprs730880566
PheGenIrs730880566
hapmaprs730880566
1000 genomesrs730880566
hgdprs730880566
ensemblrs730880566
gopubmedrs730880566
geneviewrs730880566
scholarrs730880566
googlers730880566
pharmgkbrs730880566
gwascentralrs730880566
openSNPrs730880566
23andMers730880566
23andMe allrs730880566
SNP Nexus

SNPshotrs730880566
SNPdbers730880566
MSV3drs730880566
GWAS Ctlgrs730880566
Max Magnitude0
ClinVar
Risk rs730880566(A;A)
Alt rs730880566(A;A)
Reference rs730880566(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359130C>T
CLNSRC
CLNACC RCV000158156.1,