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rs730880602

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880602(A;G)
Make rs730880602(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47332134
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880602
ebirs730880602
HLIrs730880602
Exacrs730880602
Varsomers730880602
Maprs730880602
PheGenIrs730880602
hapmaprs730880602
1000 genomesrs730880602
hgdprs730880602
ensemblrs730880602
gopubmedrs730880602
geneviewrs730880602
scholarrs730880602
googlers730880602
pharmgkbrs730880602
gwascentralrs730880602
openSNPrs730880602
23andMers730880602
23andMe allrs730880602
SNP Nexus

SNPshotrs730880602
SNPdbers730880602
MSV3drs730880602
GWAS Ctlgrs730880602
Max Magnitude0
ClinVar
Risk rs730880602(G;G)
Alt rs730880602(G;G)
Reference rs730880602(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYBPC3
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.47353685T>C
CLNSRC
CLNACC RCV000168825.2,