Table 1.
Empirical powers for DBP causal variants.
Characteristics | No correction | Bonferroni correction | |||||||
---|---|---|---|---|---|---|---|---|---|
SNP | Gene | MAF | Effect Size | Heritability | MGA | FBAT | MGA | FBAT | FBAT-VS |
rs304079 | SUMF1 | 0.4828 | 0.0895 | 0.00005 | 0.015 | 0.010 | 0 | 0 | 0 |
rs373572 | RAD18 | 0.3707 | 0.0002 | 0 | 0.050 | 0.015 | 0 | 0 | 0 |
rs1800734 | MLH1 | 0.3190 | −0.1142 | 0.00007 | 0.005 | 0.060 | 0 | 0 | 0 |
rs2020873 | MLH1 | 0.0135 | −0.4753 | 0.00005 | 0.035 | 0* | 0 | 0* | 0* |
rs11711953 | MAP4 | 0.0261 | −6.2235 | 0.02290 | 1.000 | 0.310 | 0.995 | 0.000 | 0.370 |
rs1131356 | FLNB | 0.4955 | 0.3875 | 0.00085 | 0.180 | 0.090 | 0 | 0 | 0 |
rs3772985 | DNASE1L3 | 0.1983 | −0.0795 | 0.00003 | 0.015 | 0.015 | 0 | 0 | 0 |
rs12491947 | DNASE1L3 | 0.0766 | 0.0005 | 0 | 0.020 | 0 | 0 | 0 | 0 |
rs9815775 | DNASE1L3 | 0.3103 | 0.037 | 0.00001 | 0.015 | 0.060 | 0 | 0 | 0 |
rs2322142 | PROK2 | 0.4234 | −0.0678 | 0.00003 | 0.015 | 0.015 | 0 | 0 | 0 |
rs6438503 | B4GALT4 | 0.1595 | −0.1248 | 0.00004 | 0.020 | 0.025 | 0 | 0 | 0 |
rs6805930 | B4GALT4 | 0.0496 | 0.1855 | 0.00004 | 0.055 | 0.005 | 0 | 0 | 0 |
rs4679394 | MUC13 | 0.1897 | −0.0891 | 0.00003 | 0.035 | 0.015 | 0 | 0 | 0 |
rs9814557 | PPP2R3A | 0.1293 | 0.0057 | 0 | 0.020 | 0.005 | 0 | 0 | 0 |
rs9826032 | PPP2R3A | 0.0135 | 0.0006 | 0 | 0.055 | 0* | 0 | 0* | 0* |
rs4683602 | ZBTB38 | 0.2716 | 0.0725 | 0.00003 | 0.220 | 0.105 | 0 | 0 | 0 |
rs16851435 | ZBTB38 | 0.2432 | −0.0041 | 0 | 0.405 | 0.140 | 0 | 0 | 0 |
Results from 200 Genetic Analysis Workshop (GAW) simulations for MGA, FBAT and FBAT-VS (the FBAT top 10 screening approach). SNPs conferring at least 20% power for any method are indicated in bold. The gene, minor allele frequency (MAF; estimated from founders), effect size, and heritability are provided. Results without multiple testing correction are listed under "No correction." Methods with a genome-wide correction are under "Bonferroni correction." Entries marked with an asterisk (*) were not tested with FBAT methods because of a lack of informative families.