Additional file 2 of Deep multiview learning to identify imaging-driven subtypes in mild cognitive impairment

Additional file 2: Table S1.Results for genetic association analysis in Fig. 9 sorted by chromosome number.Thresholding at p= 0.05 with FDR correction, only SNPs that are significant in at least one case control associationtest are included and only p-values for significant results are recorded. Mapped gene(s) for each SNP are shown asthey are recorded in GWAS Catalog - SNPs in multiple genes are separated by comma, interactions are separated by”x”, and upstream anddownstream genes are separated by a hyphen for intergenic SNPs.