TABLE 3.
Adjusted mean (± SE) TRIG levels for SNPs that showed significant associations with TRIG after adjusting for multiple comparisons
| Adjusted Means ± SE |
Variation in TRIG Explained by SNP | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Gene Name | SNP rs no. | Chromosome | Position (bp)* | Study Population | 1/1 | 1/2 | 2/2 | Additive P-value | |
| HNF4A | rs3746575a | 20 | 42491510 | Family | 82 ± 4.3 | 93 ± 3.3 | 114 ± 6.6 | 6.7% | 0.0006 |
| Population-based | 111 ± 2.6 | 112 ± 2.0 | 109 ± 2.9 | 0.21 | 0.57 | ||||
| HNF4A | rs11574739 | 20 | 42476364 | Family | 88 ± 3.1 | 94 ± 4.3 | 146 ± 11.7 | 5.7% | 0.0012 |
| Population-based | 112 ± 1.7 | 110 ± 2.5 | 110 ± 6.9 | 0.16 | 0.47 | ||||
| HNF4A | rs1028583 | 20 | 42484175 | Family | 85 ± 4.3 | 91 ± 3.4 | 112 ± 6.4 | 4.5% | 0.0015 |
| Population-based | 111 ± 2.6 | 111 ± 1.9 | 110 ± 2.9 | 0.011 | 0.96 | ||||
| HNF4A | rs3212198 | 20 | 42477776 | Family | 84 ± 3.9 | 93 ± 3.6 | 112 ± 6.5 | 5.1% | 0.0019 |
| Population-based | 112 ± 2.3 | 110 ± 2.0 | 112 ± 3.2 | 0.03% | 0.78 | ||||
| HNF4A | rs6073435 | 20 | 42487002 | Family | 87 ± 3.7 | 92 ± 3.6 | 119 ± 7.6 | 4.3% | 0.0025 |
| Population-based | 113 ± 2.2 | 109 ± 2.0 | 114 ± 3.4 | 0.11% | 0.87 | ||||
| LDLR | rs2569540 | 19 | 11099239 | Family | 106 ± 4.7 | 90 ± 3.6 | 83 ± 5.1 | 3.6% | 0.001 |
| Population-based | 114 ± 2.5 | 114 ± 20.0 | 111 ± 3.19 | 0.38 | 0.20 | ||||
| LDLR | rs5927 | 19 | 11094941 | Family | 86 ± 3.7 | 95 ± 3.9 | 108 ± 7.2 | 3.5% | 0.0023 |
| Population-based | 111 ± 2.0 | 112 ± 2.1 | 108 ± 4.3 | 0.28% | 0.76 | ||||
| AdipoR2 | rs11608456 | 12 | 1701455 | Family | 97 ± 2.9 | 79 ± 5.3 | 70 ± 18.3 | 3.8% | 0.0007 |
| Population-based | ND | ND | ND | ND | ND | ||||
| LPIN1 | rs11890442 | 2 | 11828454 | Family | 85 ± 3.2 | 98 ± 4.3 | 119 ± 7.6 | 6.1% | 0.0009 |
| Population-based | 111 ± 2.0 | 110 ± 2.1 | 118 ± 4.1 | 0.61 | 0.31 | ||||
1, Major allele; 2, minor allele.
In the population-based Afro-Caribbean replication study rs6031593 was genotyped as a proxy SNP for rs3746575 genotyped in the family study. Bold indicates significant P-value. ND, Not determined due to assay failure.
* Chromosomal position was based on the National Center for Biotechnology Information dbSNP, build 36.2.