Table 4.
Glycan Peak | Model | rs6573604 | rs11621121 | rs10483776 | rs4073416 | Haplo-Type | ||||
---|---|---|---|---|---|---|---|---|---|---|
H/U * | p | H/U * | p | H/U * | p | H/U * | p | |||
GP08 (A2G2) | Genetic | 0.06 | 0.999 | 9.06 | 0.215 | 2.95 | 0.593 | 10.26 | 0.117 | H = 26.75; p = 0.101 |
Allelic | 20754.5 | 0.978 | 25454.0 | 0.059 | 17330.5 | 0.333 | 24352.0 | 0.020 | ||
GP14 (A2G2S1) | Genetic | 0.62 | 0.893 | 4.61 | 0.650 | 5.24 | 0.475 | 9.85 | 0.091 | H = 21.39; p = 0.351 |
Allelic | 19956.5 | 0.726 | 26820.0 | 0.254 | 16446.5 | 0.202 | 24472 | 0.013 | ||
GP22 (FA2G2S2) | Genetic | 1.56 | 0.744 | 21.00 | 0.001 | 22.05 | <0.001 | 14.61 | 0.039 | H = 31.41; p < 0.001 |
Allelic | 19856.5 | 0.710 | 23408.0 | 0.001 | 13506.5 | <0.001 | 23952 | 0.016 | ||
GP29 (FA3G3S3) | Genetic | 3.99 | 0.530 | 4.07 | 0.464 | 12.85 | 0.020 | 6.99 | 0.234 | H = 28.37; p = 0.020 |
Allelic | 18026.5 | 0.167 | 27664.0 | 0.333 | 14608.5 | 0.003 | 25248 | 0.068 | ||
GP31 (FA3G3S3) | Genetic | 3.94 | 0.493 | 8.69 | 0.169 | 24.36 | <0.001 | 1.29 | 0.757 | H = 41.19; p < 0.001 |
Allelic | 18042.5 | 0.151 | 25588.0 | 0.052 | 13052.5 | <0.001 | 27646 | 0.397 | ||
GP34 (A4G4S3) | Genetic | 6.66 | 0.281 | 2.57 | 0.540 | 13.53 | 0.013 | 1.38 | 0.755 | H = 14.39; p = 0.013 |
Allelic | 17340.5 | 0.068 | 27578.0 | 0.345 | 14452.5 | 0.002 | 28230 | 0.559 | ||
GP36 (A4G4S4) | Genetic | 15.13 | 0.020 | 4.58 | 0.563 | 1.44 | 0.702 | 0.41 | 0.881 | H = 23.30; p = 0.256 |
Allelic | 16010.5 | 0.003 | 26752.0 | 0.341 | 18606.5 | 0.781 | 28718 | 0.706 | ||
GP37 (A4G4S4) | Genetic | 15.14 | 0.013 | 0.10 | 0.978 | 3.50 | 0.522 | 0.18 | 0.912 | H = 35.03; p = 0.316 |
Allelic | 15514.5 | 0.001 | 29586.0 | 0.876 | 16828.5 | 0.273 | 28868 | 0.743 | ||
GP38 (A4G4S4) | Genetic | 17.40 | 0.007 | 0.85 | 0.728 | 1.62 | 0.666 | 0.23 | 0.914 | H = 33.42; p = 0.440 |
Allelic | 15342.5 | 0.001 | 28706.0 | 0.585 | 17988.5 | 0.622 | 29370 | 0.980 |
* Data analyzed using the Kruskal–Wallis ANOVA of ranks for the genetic model and represented with the H value, or the Mann–Whitney U test for the allelic model and represented with the U value. Significant p-values (corrected using the Benjamini–Hochberg procedure) are denoted in bold.