Additional file 1 of Common and rare variant analyses implicate late-infancy cerebellar development and immune genes in ADHD

Supplementary Material 1: Table S1. Demographic characteristics of cases and unrelated samples. Table S2. Results for the 41 identified index variants in the current GWAS and PGC ADHD. Table S3. Results from candidate gene-based association analysis by MAGMA. Table S4. Genes mapped to independent risk loci in FUMA. Table S5. Associations of suggestive ADHD GWAS signals with other traits from PhenoScanner. Table S6. Functional annotations of tested low-frequency / rare variants in association analysis.

补充材料1：
表S1 病例与无关对照样本的人口统计学特征
表S2 本次全基因组关联研究（Genome-Wide Association Study，GWAS）与精神疾病基因组学联合会（Psychiatric Genomics Consortium，PGC）注意缺陷多动障碍（Attention-Deficit/Hyperactivity Disorder，ADHD）中鉴定出的41个索引变异的分析结果
表S3 采用MAGMA开展的候选基因关联分析结果
表S4 FUMA分析中定位到独立风险位点的基因
表S5 提示性注意缺陷多动障碍全基因组关联研究信号与PhenoScanner数据库中其他性状的关联分析结果
表S6 关联分析中检测到的低频/罕见变异的功能注释结果