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rs730880669

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs730880669(-;C)
Make rs730880669(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333306
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880669
ClinGenrs730880669
ebirs730880669
HLIrs730880669
Exacrs730880669
Varsomers730880669
Maprs730880669
PheGenIrs730880669
hapmaprs730880669
1000 genomesrs730880669
hgdprs730880669
ensemblrs730880669
gopubmedrs730880669
geneviewrs730880669
scholarrs730880669
googlers730880669
pharmgkbrs730880669
gwascentralrs730880669
openSNPrs730880669
23andMers730880669
23andMe allrs730880669
SNP Nexus

SNPshotrs730880669
SNPdbers730880669
MSV3drs730880669
GWAS Ctlgrs730880669
Max Magnitude0
ClinVar
Risk rs730880669(C;C)
Alt rs730880669(C;C)
Reference Rs730880669(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354858dupG
CLNSRC
CLNACC RCV000223712.1,