Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13146272
rs13146272
CYP4V2
CUI: C1861172
Disease: Venous Thromboembolism
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
CYP4V2
CUI: C1861172
Disease: Venous Thromboembolism
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
CYP4V2
CUI: C1861172
Disease: Venous Thromboembolism
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