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rs730880619

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880619(C;C)
Make rs730880619(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47350024
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880619
ebirs730880619
HLIrs730880619
Exacrs730880619
Varsomers730880619
Maprs730880619
PheGenIrs730880619
hapmaprs730880619
1000 genomesrs730880619
hgdprs730880619
ensemblrs730880619
gopubmedrs730880619
geneviewrs730880619
scholarrs730880619
googlers730880619
pharmgkbrs730880619
gwascentralrs730880619
openSNPrs730880619
23andMers730880619
23andMe allrs730880619
SNP Nexus

SNPshotrs730880619
SNPdbers730880619
MSV3drs730880619
GWAS Ctlgrs730880619
Max Magnitude0
ClinVar
Risk rs730880619(C;C)
Alt rs730880619(C;C)
Reference rs730880619(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47371575C>G
CLNSRC
CLNACC RCV000158286.2,