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. 2020 Jan 7;15(1):e0227357. doi: 10.1371/journal.pone.0227357

Table 3. Significant variants associated with hypertriglyceridemia (TG ≥150 mg/dL).

Chr SNP Position Gene M Discovery set Replication set
MAF OR P MAF OR P
(case / control) (95% CI) (case / control) (95% CI)
2 rs780092 27743154 GCKR G 0.275 / 0.334 0.752 4.82×10−9 0.279 / 0.336 0.753 1.19×10−3
(0.683–0.827) (0.635–0.894)
2 rs780093 27742603 GCKR C 0.395 / 0.471 0.730 2.55×10−12 0.398 / 0.474 0.721 5.47×10−5
(0.669–0.797) (0.615–0.845)
2 rs780094 27741237 GCKR C 0.397 / 0.472 0.736 6.49×10−12 0.400 / 0.475 0.723 5.91×10−5
(0.674–0.803) (0.617–0.847)
2 rs1260326 27730940 GCKR C 0.385 / 0.460 0.731 3.89×10−12 0.392 / 0.463 0.729 1.07×10−4
(0.669–0.799) (0.622–0.856)
2 rs1260333 27748624 GCKR G 0.392 / 0.468 0.734 5.20×10−12 0.392 / 0.472 0.704 1.75×10−5
(0.672–0.802) (0.600–0.827)
2 rs1919127 27801493 C2orf16 T 0.417 / 0.477 0.776 1.18×10−8 0.420 / 0.491 0.755 3.67×10−4
(0.711–0.846) (0.646–0.881)
2 rs1919128 27801759 C2orf16 A 0.415 / 0.476 0.772 7.39×10−9 0.419 / 0.491 0.754 3.65×10−4
(0.707–0.843) (0.646–0.881)
11 rs662799 116663707 APOA5 G 0.391 / 0.278 1.770 4.97×10−34 0.389 / 0.277 1.732 8.49×10−11
(1.614–1.94) (1.467–2.045)
11 rs2075291 116661392 APOA5 A 0.117 / 0.068 1.940 3.67×10−19 0.106 / 0.069 1.739 6.93×10−5
(1.678–2.243) (1.324–2.284)
11 rs2266788 116660686 APOA5 G 0.273 / 0.209 1.482 9.26×10−15 0.281 / 0.207 1.538 4.03×10−6
(1.342–1.637) (1.281–1.846)
11 rs603446 116654435 ZPR1 T 0.191 / 0.242 0.726 6.24×10−9 0.178 / 0.231 0.705 5.48×10−4
(0.651–0.809) (0.578–0.860)
11 rs964184 116648917 ZPR1 G 0.271 / 0.208 1.479 1.47×10−14 0.279 / 0.205 1.552 2.93×10−6
(1.339–1.634) (1.291–1.866)
11 rs2075295 116628401 BUD13 C 0.404 / 0.466 0.755 4.56×10−10 0.424 / 0.480 0.793 4.04×10−3
(0.691–0.825) (0.677–0.929)
11 rs11216126 116617240 BUD13 C 0.150 / 0.205 0.666 1.34×10−11 0.177 / 0.206 0.808 3.70×10−2
(0.592–0.749) (0.661–0.987)
11 rs1558861 116607437 BUD13 C 0.275 / 0.213 1.463 5.85×10−14 0.278 / 0.212 1.463 4.37×10−5
(1.325–1.616) (1.219–1.756)

Chr, chromosome; rs number, SNP ID in dbSNP database; M, minor allele; MAF, minor allele frequency; OR, odds ratio; CI, confidence interval, respectively