Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2036914
rs2036914
F11
C 0.830 GeneticVariation GWASCAT Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism. 31420334

2019
dbSNP: rs2036914
rs2036914
F11
0.830 GeneticVariation BEFREE Our findings suggest that the risk of VTE by FHMI is not explained by rs8176719 (ABO), rs6025 (F5), rs1799963 (F2), rs2066865 (FGG), and rs2036914 (F11). 31124268

2019
dbSNP: rs2036914
rs2036914
F11
0.830 GeneticVariation BEFREE The meta-analysis revealed that the F11 rs2289252, F11 rs2036914, FGG rs2066865, and CYP4V2 rs13146272 polymorphisms were closely related to the development of VTE in the white race under the best genetic models after multiple testing adjustments. 28353616

2017
dbSNP: rs2036914
rs2036914
F11
0.830 GeneticVariation BEFREE In F11, the CC genotype for rs2036914 and the CT and TT genotypes for rs2289252 were associated with a significantly higher VTE risk. 23150947

2013
dbSNP: rs2036914
rs2036914
F11
0.830 GeneticVariation GWASDB Genetics of venous thrombosis: insights from a new genome wide association study. 21980494

2011