Table 1.
rsID | Chr | Position (hg19) | Nearby gene | EA | NEA | EAF | Beta | SE | P | Included in main analysis |
rs2857602 | 6 | 31,533,378 | LTA | G | A | 0.38 | 0.032 | 0.006 | 3.30 × 10−12 | No |
rs10744774 | 12 | 112,090,022 | BRAP | A | C | 0.83 | 0.044 | 0.007 | 6.94 × 10−11 | Yes |
rs3184504 | 12 | 111,884,608 | SH2B3 | T | C | 0.48 | 0.030 | 0.005 | 3.96 × 10−10 | Yes |
rs7182229 | 15 | 58,765,183 | LIPC | T | G | 0.11 | 0.050 | 0.009 | 1.07 × 10−9 | Yes |
Chr indicates chromosome; EA; effect allele; EAF, effect allele frequency; NEA, non-effect allele; SE, standard error; TNF, tumour necrosis factor. Rs2857602 was not included in the main analysis since the TNF-increasing allele was associated with lower odds of rheumatoid arthritis and inflammatory bowel disease.