Table 2.
Phenotype | SNPID [chr:position:ref:alt] (rsid) | Most severe consequence | Original GWAS results | Conditional results | ||
---|---|---|---|---|---|---|
OR [CI] | p-value | OR [CI] | p-value | |||
Coronary atherosclerosis | chr15:88901702:C:CTGT (rs534125149) | Inframe insertion | 0.75 [0.71–0.81] | 2.63 × 10−16 | 0.75 [0.70–0.80]a | 7.68 × 10−15a |
chr15:88899813:T:G (rs201988637) | Splice acceptor variant | 0.72 [0.63–0.83] | 7.94 × 10−6 | 0.73 [0.64–0.85]b | 1.99 × 10−5b | |
Myocardial infarction, strict | chr15:88901702:C:CTGT (rs534125149) | Inframe insertion | 0.74 [0.68–0.81] | 1.95 × 10−11 | 0.79 [0.73–0.85]a | 1.92 × 10−10a |
chr15:88899813:T:G (rs201988637) | Splice acceptor variant | 0.69 [0.58–0.83] | 9.62 × 10−5 | 0.71 [0.59–0.85]b | 4.03 × 10−4b |
This table present the conditional analysis results for coronary atherosclerosis and MI (strict definition, only primary diagnoses accepted) where the association has been conditioned on rs534125149 and rs201988637, separately.
aConditional on rs201988637.
bConditional on rs534125149.