Table 4.
SNP | Minor | Major | Freq (affected) | Freq (unaffected) | Unadjusted | Adjusted (baseline) | Adjusted (ancestry) | Emergent symptoms | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
χ 2 | p | OR | 95% CI | p | OR | p | OR | p (sex heterogeneity) | p | OR | |||||
rs10515697 | T | A | 0.31 | 0.26 | 8.189 | 0.0042 | 1.28 | 1.08, 1.51 | 0.0123 | 1.26 | 0.0139 | 1.25 | 0.4813 | 0.0005 | 1.49 |
rs1994862 | C | G | 0.31 | 0.26 | 8.104 | 0.0044 | 1.27 | 1.08, 1.51 | 0.0132 | 1.25 | 0.0146 | 1.24 | 0.4968 | 0.0006 | 1.48 |
rs1864205 | G | A | 0.36 | 0.32 | 5.636 | 0.0176 | 1.21 | 1.03, 1.42 | 0.0836 | 1.16 | 0.0628 | 1.16 | 0.9275 | 0.0391 | 1.26 |
Column headings refer to unadjusted association, association adjusted for baseline clinical features, association adjusted for ancestry-informative markers, test for heterogeneity between men and women, and association with only confirmed emergent symptoms (ie those not present at initial follow-up visit).