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rs730880634

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880634(G;G)
Make rs730880634(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346205
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880634
ebirs730880634
HLIrs730880634
Exacrs730880634
Varsomers730880634
Maprs730880634
PheGenIrs730880634
hapmaprs730880634
1000 genomesrs730880634
hgdprs730880634
ensemblrs730880634
gopubmedrs730880634
geneviewrs730880634
scholarrs730880634
googlers730880634
pharmgkbrs730880634
gwascentralrs730880634
openSNPrs730880634
23andMers730880634
23andMe allrs730880634
SNP Nexus

SNPshotrs730880634
SNPdbers730880634
MSV3drs730880634
GWAS Ctlgrs730880634
Max Magnitude0
ClinVar
Risk rs730880634(G;G)
Alt rs730880634(G;G)
Reference rs730880634(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47367756A>C
CLNSRC
CLNACC RCV000158331.1,