Table 3.
31 of the 113 novel loci (P < 5 × 10−8) identified with PP as the primary trait
| SNP | CHR:BP | Trait | Gene | A1 | A2 | EAF | Effect | s.e. | P value | neff | Phet |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34361301 | 9:14535119 | PP | NFIB | C | T | 0.266 | 0.122 | 0.02 | 6.76 × 10−10 | 974,146 | 0.322 |
| rs34139656 | 16:88534923 | PP | ZFPM1 | G | A | 0.327 | −0.117 | 0.019 | 7.30 × 10−10 | 939,836 | 0.819 |
| rs300753 | 2:209622 | PP | SH3YL1 | T | C | 0.548 | 0.106 | 0.017 | 1.06 × 10−9 | 975,060 | 0.487 |
| rs61241090 | 9:35191014 | PP | UNC13B | C | T | 0.236 | −0.123 | 0.02 | 1.40 × 10−9 | 991,997 | 0.658 |
| rs116643984 | 15:101791212 | PP | CHSY1 | A | C | 0.163 | −0.143 | 0.024 | 2.45 × 10−9 | 954,926 | 0.806 |
| rs2987903 | 9:133711263 | PP | ABL1 | A | G | 0.128 | −0.154 | 0.026 | 2.49 × 10−9 | 995,802 | 0.631 |
| rs4944038 | 11:73783478 | PP | C2CD3 | T | A | 0.477 | −0.101 | 0.017 | 4.30 × 10−9 | 1,006,450 | 0.33 |
| rs3821817 | 3:187456904 | PP | BCL6 | G | C | 0.178 | −0.135 | 0.023 | 4.59 × 10−9 | 944,591 | 0.274 |
| rs77759442 | 11:110657616 | PP | ARHGAP20 | T | C | 0.132 | 0.15 | 0.026 | 5.91 × 10−9 | 960,047 | 0.358 |
| rs75177877 | 7:16117030 | PP | CRPPA | T | C | 0.172 | 0.136 | 0.024 | 7.02 × 10−9 | 941,294 | 0.169 |
| rs62253186 | 3:69919744 | PP | MITF | G | C | 0.061 | 0.217 | 0.038 | 7.14 × 10−9 | 920,630 | 0.94 |
| rs4517643 | 13:94417873 | PP | GPC6 | C | A | 0.566 | 0.101 | 0.018 | 7.47 × 10−9 | 990,764 | 0.633 |
| rs12828693 | 12:46385848 | PP | SCAF11 | T | C | 0.205 | 0.125 | 0.022 | 8.20 × 10−9 | 970,335 | 0.806 |
| rs4053778 | 6:85988429 | PP | LINC02535 | G | A | 0.395 | −0.103 | 0.018 | 8.67 × 10−9 | 968,001 | 0.332 |
| rs71664847 | 1:115019239 | PP | TRIM33 | T | A | 0.19 | 0.126 | 0.022 | 9.99 × 10−9 | 993,341 | 0.633 |
| rs12134085 | 1:40763095 | PP | COL9A2 | T | C | 0.198 | −0.133 | 0.023 | 1.05 × 10−8 | 864,823 | 0.003 |
| rs9320778 | 6:121258543 | PP | TBC1D32 | T | C | 0.75 | 0.115 | 0.02 | 1.05 × 10−8 | 973,244 | 0.75 |
| rs112324977 | 9:80751434 | PP | CEP78 | A | T | 0.131 | −0.147 | 0.026 | 1.07 × 10−8 | 992,833 | 0.763 |
| rs72751391 | 9:122890934 | PP | MIR147A | T | C | 0.125 | 0.156 | 0.027 | 1.23 × 10−8 | 907,738 | 0.942 |
| rs10208493 | 2:196590414 | PP | SLC39A10 | T | C | 0.571 | −0.099 | 0.017 | 1.36 × 10−8 | 986,727 | 0.186 |
| rs2953937 | 8:34164285 | PP | LINC01288 | C | A | 0.133 | 0.143 | 0.026 | 1.76 × 10−8 | 993,180 | 0.135 |
| rs36036692 | 8:108319395 | PP | ANGPT1 | G | C | 0.374 | 0.1 | 0.018 | 1.89 × 10−8 | 997,711 | 0.167 |
| rs12943001 | 17:78238645 | PP | RNF213 | C | T | 0.641 | −0.111 | 0.02 | 2.29 × 10−8 | 830,757 | 0.064 |
| rs67615620 | 7:15421023 | PP | AGMO | C | T | 0.199 | 0.122 | 0.022 | 2.32 × 10−8 | 973,513 | 0.463 |
| rs9554446 | 13:98859019 | PP | FARP1 | A | T | 0.095 | 0.166 | 0.03 | 2.32 × 10−8 | 974,068 | 0.586 |
| rs9671694 | 14:103330144 | PP | TRAF3 | G | C | 0.337 | 0.104 | 0.019 | 2.40 × 10−8 | 961,925 | 0.743 |
| rs72943226 | 6:99548729 | PP | MIR548AI | A | G | 0.319 | 0.102 | 0.018 | 3.12 × 10−8 | 999,371 | 0.245 |
| rs1062298 | 12:12045264 | PP | ETV6 | T | G | 0.421 | 0.097 | 0.018 | 3.24 × 10−8 | 977,558 | 0.084 |
| rs855791 | 22:37462936 | PP | TMPRSS6 | G | A | 0.563 | −0.096 | 0.017 | 3.24 × 10−8 | 996,826 | 0.861 |
| rs12084868 | 1:72229240 | PP | NEGR1 | A | G | 0.028 | 0.302 | 0.055 | 4.67 × 10−8 | 898,662 | 0.546 |
| rs11022023 | 11:11793978 | PP | MIR8070 | A | G | 0.083 | −0.174 | 0.032 | 4.80 × 10−8 | 964,778 | 0.539 |
31 of the 113 novel loci (P < 5 × 10−8) with concordant direction of effect in all available studies after distance-based (±500 kb) and LD (r2 > 0.1) pruning, identified with PP as the primary trait. SNPs are ordered by two-sided P value for the most significant BP association in inverse variance-weighted meta-analyses. SNP, dbSNP accession number; CHR:BP, chromosome and build 37 position; Trait, primary BP trait for which the most significant association was observed and for which summary statistics are provided in subsequent columns; for novel loci which reach genome-wide significance (P < 5 × 10−8) for a second trait, this second trait is also listed; Nearest Gene, most proximal gene within 250 kb of sentinel SNP; A1, allele corresponding to measured effect on the outcome; A2, allele not corresponding to measured effect on the outcome; EAF, effect allele frequency in the meta-analysis; Effect, measured effect in the meta-analysis (mmHg); s.e., standard error of the measured effect in the meta-analysis; P value, association P value for the measured effect in the meta-analysis; neff, effective number of subjects in the GWAS meta-analysis (calculated at study-level as n × SNP imputation quality INFO); Phet, value for Cochran’s Q test of statistical heterogeneity in the GWAS meta-analysis.