Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE When we considered the risk of IS within 2 years under VKA treatment, we found that only the rs21</span>08622 AA genotype was significantly associated with this endpoint (early IS) (hazard ratio 6.81, 95% CI 1.37-33.92, p = 0.019). 29273767

2018

dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE CYP4A1l rs9333025 GG and CYP4F2 rs2108622 GG two-loci interaction significantly increases the risk for IS and an elevated 20-HETE level. 26959478

2016

dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE Haplotype analysis indicated that the GGGT haplotype comprising rs2108622-rs3093100-rs3093105-rs3093135 was associated with IS, which suggests that the GGGT haplotype may be a risk factor for IS (P = 0.012). 25730002

2015

dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE Interestingly, the effects of CYP4F2 V433M</span> on ischemic stroke in our study was only evident in male individuals. 20130494

2010

dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE The present study aimed to evaluate whether or not the CYP4F2 gene polymorphism V433M (rs2108622) is involved in ischemic stroke in the Northern Chinese Han population. 20227456

2010

dbSNP: rs2108622
rs2108622
0.060 GeneticVariation BEFREE The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure. 18574070

2008