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rs786205481

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205481(C;T)
Make rs786205481(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position24912893
GeneCENPJ
is asnp
is mentioned by
dbSNPrs786205481
dbSNP (old)rs786205481
ClinGenrs786205481
ebirs786205481
HLIrs786205481
Exacrs786205481
Gnomadrs786205481
Varsomers786205481
Maprs786205481
PheGenIrs786205481
Biobankrs786205481
1000 genomesrs786205481
hgdprs786205481
ensemblrs786205481
gopubmedrs786205481
geneviewrs786205481
scholarrs786205481
googlers786205481
pharmgkbrs786205481
gwascentralrs786205481
openSNPrs786205481
23andMers786205481
23andMe allrs786205481
SNP Nexus

SNPshotrs786205481
SNPdbers786205481
MSV3drs786205481
GWAS Ctlgrs786205481
Max Magnitude0
ClinVar
Risk rs786205481(T;T)
Alt rs786205481(T;T)
Reference Rs786205481(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CENPJ
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.25487031G>A
CLNSRC
CLNACC RCV000171216.1,