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rs730880691

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880691(A;A)
Make rs730880691(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342573
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880691
ebirs730880691
HLIrs730880691
Exacrs730880691
Varsomers730880691
Maprs730880691
PheGenIrs730880691
hapmaprs730880691
1000 genomesrs730880691
hgdprs730880691
ensemblrs730880691
gopubmedrs730880691
geneviewrs730880691
scholarrs730880691
googlers730880691
pharmgkbrs730880691
gwascentralrs730880691
openSNPrs730880691
23andMers730880691
23andMe allrs730880691
SNP Nexus

SNPshotrs730880691
SNPdbers730880691
MSV3drs730880691
GWAS Ctlgrs730880691
Max Magnitude0
ClinVar
Risk rs730880691(A;A)
Alt rs730880691(A;A)
Reference rs730880691(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47364124C>T
CLNSRC
CLNACC RCV000158432.1,