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. 2020 Mar 20;28(8):1056–1065. doi: 10.1038/s41431-020-0603-2

Table 3.

PRSice-2 polygenic risk score (PRS) prediction results for UK Biobank target samples, for optimal p value threshold.

Measure pair Target sample Threshold PRS R2 Full R2 Null R2 Coefficient Standard error p No. of SNP Empirical p
HAID–HAID AA 0.36 0.0104 0.0248 0.0144 112,697 40,950.5 0.0059 132,397 0.0701
HAID–HD AA 0.017 0.0033 0.0991 0.0958 −7664.44 2951.83 0.0094 11,338 1
HD–HAID AA 0.016 0.0015 0.0159 0.0144 4257.94 4092.96 0.2982 15,955 1
HD–HD AA 0.019 0.0006 0.0964 0.0958 −2025.13 1827.21 0.2677 17,932 1
HAID–HAID CH 0.14005 0.0041 0.0212 0.0172 31,395.8 27,561.6 0.2547 42,704 1
HAID–HD CH 0.0003 0.0025 0.0687 0.0662 −730.731 569.454 0.1994 317 1
HD–HAID CH 0.0091 0.0210 0.0382 0.0172 10,772.2 4188.19 0.0101 7853 0.1025
HD–HD CH 0.015 0.0095 0.0757 0.0662 5924.37 2355.89 0.0119 11,034 0.1085
HAID–HAID EA 0.0092 0.0017 0.0701 0.0684 15,670.8 3775.81 3.320E−05 10,648 0.0009
HAID–HD EA 0.35 0.0013 0.0468 0.0455 53,336.3 10,047.5 1.106E−07 183,790 <0.0001
HD–HAID EA 0.019 0.0027 0.0711 0.0684 13207 2506.83 1.376E−07 24,107 <0.0001
HD–HD EA 0.018 0.0124 0.0579 0.0455 18,389.9 1111.69 1.821E−61 23,187 <0.0001
HAID–HAID SA 0.045 0.0032 0.0424 0.0392 −19,437.9 7590.78 0.0104 28,737 1
HAID–HD SA 0.1 0.0007 0.0457 0.0450 −9085.58 5864.3 0.1213 55,832 1
HD–HAID SA 0.0037 0.0014 0.0407 0.0392 −2137.48 1241.07 0.0850 5932 1
HD–HD SA 0.28005 0.0075 0.0525 0.0450 24,413.7 4746.59 2.698E−07 123,566 <0.0001

Measure pair denotes base sample polygenic risk scores constructed from UK Biobank genome-wide association study on British samples of either wearing a hearing aid (HAID) or having hearing difficulties (HD), respectively, predicting the UK Biobank target phenotypes HAID and HD, respectively. Target sample refers to the four UK Biobank subpopulations, African (AA), Chinese (CH), European (EA), and South Asian (SA), described in the text. Threshold is the p value threshold for SNP inclusion that maximised variance explained in the respective target phenotype. PRS R2 is the variance in the target phenotype explained by the PRS. Full R2 is the variance explained by the full-model regression, which includes the PRS as well as the covariates age and sex, while Null R2 does not include the PRS, just the covariates. Coefficient is the regression coefficient for the PRS term, with standard error and p its corresponding standard error and p value. No. of SNP is the number of SNPs included in the PRS and empirical p is the p value obtained from simulation, which corrects for both multiple thresholds tested in order to obtain the optimal threshold and for relatedness in the sample, such as the inclusion of DZ twin pairs.