TABLE 1.
ID a | rsID | Closest gene | Discovery | Replication | Meta‐analysis (discovery and replication) | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|
OR (95% CI) | p | Cochran's Q p | OR (95% CI) | p | Cochran's Q p | OR (95% CI) | p | Cochran's Q p | |||
1:101210560:C:T | rs12091010 | EXTL2 | 0.82 (0.75–0.90) | 9.05E‐06 | 4.83E‐01 | 0.89 (0.82–0.97) | 5.35E‐03 | 4.92E‐01 | 0.86 (0.81–0.91) | 4.23E‐07 | 4.47E‐01 |
5:22659406:T:C | rs6888198 | CDH12 | 1.37 (1.23–1.54) | 1.95E‐08 | 5.82E‐01 | 1.02 (0.90–1.15) | 7.72E‐01 | 7.18E‐01 | 1.24 (1.05–1.45) | 2.41E‐06 | 1.89E‐02 |
10:91376299:T:C | rs943126 | PANK1 | 0.85 (0.78–0.92) | 3.10E‐05 | 8.01E‐02 | 0.92 (0.86–0.98) | 1.30E‐02 | 3.87E‐01 | 0.89 (0.85–0.94) | 4.93E‐06 | 7.91E‐02 |
Abbreviations: 95% CI, 95% confidence interval; OR, odds ratio; p, p‐value.
The variant identifier corresponds to chromosomal position (hg19) followed by non‐tested allele and tested allele.