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. 2017 May 24;8:15539. doi: 10.1038/ncomms15539

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Copyright © 2017, The Author(s)

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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Risk allele effects for the five new genome-wide significant loci in the individual case-control data sets and GWA meta-analysis: FN1 2q35 (3a), CCDC170 on 6q25.1 (3b), SYNE1 on 6q25.1 (3c), 7p12.3 (3d), and near FSHB on 11p14.1 (3e). Results for 2q35 and 7p12.3 are based on analysis including only moderate-to-severe ('Grade B') endometriosis cases. Risk allele effects of the remaining three SNPs are from analysis including all endometriosis cases.