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rs730880593

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880593(C;G)
Make rs730880593(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332652
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880593
ebirs730880593
HLIrs730880593
Exacrs730880593
Varsomers730880593
Maprs730880593
PheGenIrs730880593
hapmaprs730880593
1000 genomesrs730880593
hgdprs730880593
ensemblrs730880593
gopubmedrs730880593
geneviewrs730880593
scholarrs730880593
googlers730880593
pharmgkbrs730880593
gwascentralrs730880593
openSNPrs730880593
23andMers730880593
23andMe allrs730880593
SNP Nexus

SNPshotrs730880593
SNPdbers730880593
MSV3drs730880593
GWAS Ctlgrs730880593
Max Magnitude0
ClinVar
Risk rs730880593(G;G)
Alt rs730880593(G;G)
Reference rs730880593(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354203G>C
CLNSRC
CLNACC RCV000158243.1,