Table 1.
SNP | Chr | Position (hg 19) | Nearest gene | Effect/other alleles | EAF | Discovery GWAS | Replication | Combined | ||||
Beta (SE) | P value | Beta (SE) | P value | Beta (SE) | P value | N | ||||||
rs780094 | 2 | 27,741,237 | GCKR | T/C | 0.40 | −0.0155 (0.0026) | 3.6 × 10−9 | 0.0035 (0.0029) | 0.238 | −0.0102 (0.0019) | 1.6 × 10−7 | 98,679 |
rs350721 | 2 | 52,980,427 | ASB3 | C/G | 0.18 | 0.0206 (0.0040) | 3.2 × 10−7 | −0.0000 (0.0042) | 0.994 | 0.0109 (0.0029) | 1.9 × 10−4 | 100,859 |
rs197273 | 2 | 161,894,663 | TANK | A/G | 0.49 | −0.0141 (0.0026) | 9.8 × 10−8 | −0.0058 (0.0028) | 0.040 | −0.0103 (0.0019) | 7.4 × 10−8 | 97,631 |
rs11940694 | 4 | 39,414,993 | KLB | A/G | 0.42 | −0.0137 (0.0027) | 3.2 × 10−7 | −0.0135 (0.0030) | 5.2 × 10−6 | −0.0136 (0.0020) | 9.2 × 10−12 | 98,477 |
rs6943555 | 7 | 698,060,23 | AUTS2 | A/T | 0.29 | −0.0115 (0.0030) | 1.4 × 10−4 | −0.0070 (0.0033) | 0.032 | −0.0094 (0.0022) | 1.9 × 10−5 | 104,282 |
rs10950202 | 7 | 69,930,098 | AUTS2 | G/C | 0.16 | −0.0194 (0.0038) | 2.9 × 10−7 | −0.0015 (0.0042) | 0.720 | −0.0113 (0.0028) | 5.9 × 10−5 | 105,639 |
One SNP with the smallest P value was taken forward per region. Chr, chromosome; EAF, effect allele frequency in the discovery GWAS.