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rs730880664

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880664(-;-)
Make rs730880664(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47351294
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880664
ebirs730880664
HLIrs730880664
Exacrs730880664
Varsomers730880664
Maprs730880664
PheGenIrs730880664
hapmaprs730880664
1000 genomesrs730880664
hgdprs730880664
ensemblrs730880664
gopubmedrs730880664
geneviewrs730880664
scholarrs730880664
googlers730880664
pharmgkbrs730880664
gwascentralrs730880664
openSNPrs730880664
23andMers730880664
23andMe allrs730880664
SNP Nexus

SNPshotrs730880664
SNPdbers730880664
MSV3drs730880664
GWAS Ctlgrs730880664
Max Magnitude0
ClinVar
Risk rs730880664(;)
Alt rs730880664(;)
Reference rs730880664(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47372845delG
CLNSRC
CLNACC RCV000158386.2,