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rs730880653

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880653(-;-)
Make rs730880653(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47337482
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880653
ebirs730880653
HLIrs730880653
Exacrs730880653
Varsomers730880653
Maprs730880653
PheGenIrs730880653
hapmaprs730880653
1000 genomesrs730880653
hgdprs730880653
ensemblrs730880653
gopubmedrs730880653
geneviewrs730880653
scholarrs730880653
googlers730880653
pharmgkbrs730880653
gwascentralrs730880653
openSNPrs730880653
23andMers730880653
23andMe allrs730880653
SNP Nexus

SNPshotrs730880653
SNPdbers730880653
MSV3drs730880653
GWAS Ctlgrs730880653
Max Magnitude0
ClinVar
Risk rs730880653(;)
Alt rs730880653(;)
Reference rs730880653(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47359033delG
CLNSRC
CLNACC RCV000158366.2,