“…Then, 12 articles were excluded, including 10 articles for which genotype data were not available, 1 article for which the abstract was available, and 1 article for which the full text was not available ( Figure 1 ). Finally, we pooled the data of 59 SNPs from 11 different LncRNAs in 21 case-control studies (19 English and 2 Chinese publications) ( Guo et al, 2015 ; Guo et al, 2016 ; Han et al, 2016 ; Jin et al, 2016 ; Qiu et al, 2016 ; Wu et al, 2016 ; He and Wei, 2017 ; Jin et al, 2017 ; Zhu et al, 2017 ; Wang et al, 2018 ; Wang and Luo, 2018 ; Weng et al, 2018 ; Huang et al, 2019 ; Jia et al, 2019 ; Gao et al, 2020 ; Minn et al, 2020 ; Wang et al, 2020 ; Weng et al, 2020 ; Sun et al, 2022 ; Yao et al, 2022 ; Yi et al, 2022 ). Details of these studies and the distribution of SNPs genotype are shown in Supplementary Table S1 .…”