Gene: CPB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1361
Gene Symbol: CPB2
CPB2 		0.040 GeneticVariation disease BEFREE For genetic factors, CVT risk increased in the presence of factor V Leiden (G1691A) by 2.5-fold (1.9-3.3), protein C deficiency 10.7-fold (3.1-37.7), protein S deficiency 5.7-fold (1.4-22.4), antithrombin deficiency 3.8-fold (1.0-13.8), prothrombin (G20210A) 5.5-fold (4.0-7.27) and TAFI gene variant (C1040T) 1.6-fold (1.0-2.4). 30005273 2018
Entrez Id: 1361
Gene Symbol: CPB2
CPB2 		0.040 GeneticVariation disease BEFREE We analyzed the association between CVT and TAFI single-nucleotide polymorphisms (rs3742264, rs2146881, and rs1926447) compared to healthy controls. 29629564 2018
Entrez Id: 1361
Gene Symbol: CPB2
CPB2 		0.040 GeneticVariation disease BEFREE Our data indicate that the GTC haplotype for TAFI 505G>A/1040C>T/+1542C>G SNPs increased the risk of CVT in comparison to controls and VTE cases. 24252537 2014
Entrez Id: 1361
Gene Symbol: CPB2
CPB2 		0.040 Biomarker disease BEFREE In contrast, our study found no significant association of CVT with SNPs of the TAFI and the PZ genes. 16155788 2006