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rs730880632

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880632(C;C)
Make rs730880632(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position47346217
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880632
ebirs730880632
HLIrs730880632
Exacrs730880632
Varsomers730880632
Maprs730880632
PheGenIrs730880632
hapmaprs730880632
1000 genomesrs730880632
hgdprs730880632
ensemblrs730880632
gopubmedrs730880632
geneviewrs730880632
scholarrs730880632
googlers730880632
pharmgkbrs730880632
gwascentralrs730880632
openSNPrs730880632
23andMers730880632
23andMe allrs730880632
SNP Nexus

SNPshotrs730880632
SNPdbers730880632
MSV3drs730880632
GWAS Ctlgrs730880632
Max Magnitude0
ClinVar
Risk rs730880632(C;C)
Alt rs730880632(C;C)
Reference rs730880632(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47367768C>G
CLNSRC
CLNACC RCV000158329.2,