Disease: Venous Thromboembolism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2102575
rs2102575
Entrez Id: 3818;285440
Gene Symbol: KLKB1;CYP4V2
KLKB1;CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.700 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568 2012
dbSNP: rs3736455
rs3736455
Entrez Id: 285440
Gene Symbol: CYP4V2
CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.700 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494 2011
dbSNP: rs13146272
rs13146272
Entrez Id: 285440
Gene Symbol: CYP4V2
CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.030 GeneticVariation BEFREE In conclusion, our pooled systematic study results indicated that individuals with the A allele h</span>ad a higher risk of developing VTE than those with the C allele of the rs13146272 variant, but the risk was inconsistent among different ethnicities. 30276487 2019
dbSNP: rs13146272
rs13146272
Entrez Id: 285440
Gene Symbol: CYP4V2
CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.030 GeneticVariation BEFREE Finally, our study demonstrated the important role of rs2289252, rs2036914, rs2066865, and rs13146272 polymorphisms in the development of VTE in the white race. 28353616 2017
dbSNP: rs13146272
rs13146272
Entrez Id: 285440
Gene Symbol: CYP4V2
CYP4V2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.030 GeneticVariation BEFREE However, using this large cohort of subjects, we were able to replicate the mild effects of 2 nonsynonymous SNPs, rs1613662 in GP6 and rs13146272 in CYP4V2, recently suspected to be associated with VTE. 19278955 2009