Table 2.
Disease | SNP selection | # SNPs (PRS) | C statistic | Reference |
---|---|---|---|---|
Breast cancer | risk + GWS | 77 | 0.622 | Mavaddat et al. (2015) |
88 |
0.5411 0.5662 |
Kuchenbaecker et al. (2017) | ||
Coronary artery disease | penalized regression | 40,079 | 0.608 | Elliott et al. (2020) |
PRS: polygenic risk score, SNP: single nucleotide polymorphism, # SNP (PRS): number of SNPs included in the PRS, GWS: genome-wide significant, C statistic: Harrell’s C statistic, 1BRCA1 mutation carriers, 2BRCA2 mutation carriers.