“…The initial search strategy retrieved a total of 464 studies from all electronic databases. After reading the titles, abstracts, and full texts, we selected 26 studies ( Diamanti-Kandarakis et al, 1999 ; Marszalek et al, 2001 ; Cousin et al, 2004 ; Kahsarmiller et al, 2004 ; Tan et al, 2005 ; Bendlová et al, 2007 ; Ferk et al, 2007 ; Echiburú et al, 2008 ; Park et al, 2008 ; Jin et al, 2009 ; Unsal et al, 2009 ; Martinez-Garcia et al, 2012 ; Dasgupta et al, 2014 ; Dai et al, 2015 ; Li et al, 2015 ; Abu-Hijleh et al, 2016 ; Banerjee et al, 2016 ; Mehdizadeh et al, 2017 ; Wu et al, 2017 ; Jiao et al, 2018 ; Kaur et al, 2018 ; Bhatnager et al, 2019 ; Liu et al, 2019 ; Rahimi and Mohammadi, 2019 ; Munawar Lone et al, 2020 ; Ashraf et al, 2021 ), which included a total of 8,903 women, for inclusion in the analysis. The remaining studies were excluded: 84 were duplicates, 315 were of apparent irrelevance based on a review of abstracts and titles, four were not case-control studies, 19 lacked sufficient genotyping data, 12 included other SNPs without gene locus, two were combined with other diseases, and two had SNPs reported in less than 5 case-control study.…”