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French glioma case germline genotypes using Illumina HumanExome-12v1_A array
UK glioma case germline genotypes using Illumina HumanExome-12v1_A array
French glioma control germline genotypes using Illumina HumanExome-12v1_A array
German glioma case germline genotypes using Illumina HumanExome-12v1_A array
German glioma control germline genotypes using Illumina HumanExome-12v1_A array
To identify protein altering variants (PAVs) for glioma we analysed Illumina HumanExome BeadChip exome array data on 1,882 glioma cases and 8,079 controls from three independent European populations. In addition to single variant tests we incorporated information on the predicted functional conseque...
Data Access Committee EGAC00001000345
Meta-analysis association statistics from case-control analysis (includes imputed SNPs)
Genome-wide association studies (GWAS) have transformed our understanding of glioma susceptibility, but individual studies have had limited power to identify risk loci. We performed a meta-analysis of existing GWAS and two new GWAS, which totaled 12,488 cases and 18,169 controls. We identified five ...
Data Access Committee EGAC00001001116
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