“…The only effect revealed in our study was the association of the variant allele rs2010963 C with the decreased risk of PVVs development. Rs2010963 G>C is the most studied polymorphism in the VEGFA gene, and numerous studies have examined its association with a variety of diseases including breast, colorectal, gastric, and lung cancer, [24][25][26] osteosarcoma, 27 diabetic retinopathy 28 and nephropathy, 29 endometriosis, 30 recurrent spontaneous abortion, 31 preeclampsia, 32 vasculitis, 33 chronic immune-mediated inflammatory diseases, 34 psoriasis, 35 and osteonecrosis of the femoral head. 36 Recent meta-analyses stratified by ethnicity-revealed associations with these pathologies predominately in Asians, 26,27,29,[34][35][36] but not in Caucasians.…”