Ontology highlight
ABSTRACT:
SUBMITTER: Shete S
PROVIDER: S-EPMC4501476 | biostudies-literature | 2009 Aug
REPOSITORIES: biostudies-literature
Shete Sanjay S Hosking Fay J FJ Robertson Lindsay B LB Dobbins Sara E SE Sanson Marc M Malmer Beatrice B Simon Matthias M Marie Yannick Y Boisselier Blandine B Delattre Jean-Yves JY Hoang-Xuan Khe K El Hallani Soufiane S Idbaih Ahmed A Zelenika Diana D Andersson Ulrika U Henriksson Roger R Bergenheim A Tommy AT Feychting Maria M Lönn Stefan S Ahlbom Anders A Schramm Johannes J Linnebank Michael M Hemminki Kari K Kumar Rajiv R Hepworth Sarah J SJ Price Amy A Armstrong Georgina G Liu Yanhong Y Gu Xiangjun X Yu Robert R Lau Ching C Schoemaker Minouk M Muir Kenneth K Swerdlow Anthony A Lathrop Mark M Bondy Melissa M Houlston Richard S RS
Nature genetics 20090705 8
To identify risk variants for glioma, we conducted a meta-analysis of two genome-wide association studies by genotyping 550K tagging SNPs in a total of 1,878 cases and 3,670 controls, with validation in three additional independent series totaling 2,545 cases and 2,953 controls. We identified five risk loci for glioma at 5p15.33 (rs2736100, TERT; P = 1.50 x 10(-17)), 8q24.21 (rs4295627, CCDC26; P = 2.34 x 10(-18)), 9p21.3 (rs4977756, CDKN2A-CDKN2B; P = 7.24 x 10(-15)), 20q13.33 (rs6010620, RTEL1 ...[more]