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rs730880694

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880694(A;A)
Make rs730880694(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47342096
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880694
ebirs730880694
HLIrs730880694
Exacrs730880694
Varsomers730880694
Maprs730880694
PheGenIrs730880694
hapmaprs730880694
1000 genomesrs730880694
hgdprs730880694
ensemblrs730880694
gopubmedrs730880694
geneviewrs730880694
scholarrs730880694
googlers730880694
pharmgkbrs730880694
gwascentralrs730880694
openSNPrs730880694
23andMers730880694
23andMe allrs730880694
SNP Nexus

SNPshotrs730880694
SNPdbers730880694
MSV3drs730880694
GWAS Ctlgrs730880694
Max Magnitude0
ClinVar
Risk rs730880694(A,T;A,T)
Alt rs730880694(A,T;A,T)
Reference rs730880694(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47363647G>T
CLNSRC
CLNACC RCV000158436.1,