Table 1.
Summary of statistics of the phenotypes used to develop the PGS rank database.a
| Phenotype (mapped trait) | # PGS files | SNP info |
|---|---|---|
| Alzheimer’s disease | 23 | w: [(−0.95)–1.64]; m: 0.0013; md: 5.82e−7; sd: 0.0390 |
| Schizophrenia | 5 | w: [(−0.04)–0.05]; m: 5.61e−5; md: 8.36e−6; sd: 0.0018 |
| Cognition | 5 | w: [(−3.60)–1.68]; m: (−0.0005); md: −7e−8; sd: 0.0321 |
a
Phenotype denotes disease or trait name. #PGS files denote the count of PGS files for each PGS ID corresponding to the phenotype. SNP info refers to the aggregated information regarding the SNPs or variants in each PGS file. SNP: single nucleotide polymorphism; w: weight range; m, md, and sd denote the mean, median, and standard deviation of the weights, respectively.