Table 4.
Associated Haplotypes in (p≤0.01) the Discovery Sample
| Phenotype | Gene | Haplotype Candidate from MDR | Freq in Controls |
Freq in Cases |
Coeff | SE | P-Value* |
|---|---|---|---|---|---|---|---|
| Plaque | SERPINE1 | SNP1=rs6092; SNP2=rs2227631; SNP3=rs1050813 | |||||
| ggg (ref) | 0.49 | 0.50 | |||||
| gaa | 0.03 | 0.09 | 1.46 | 0.52 | 5.28E-03 | ||
| Thick | vWF | SNP1=rs980130; SNP2=rs216809 | |||||
| gc (ref) | 0.47 | 0.63 | |||||
| ga | 0.33 | 0.15 | −1.074 | 0.38 | 5.21E-03 | ||
| Irregular | vWF | SNP1=rs4764478; SNP2=rs2885517; SNP3=rs12580343 | |||||
| tgg (ref) | 0.3 | 0.22 | |||||
| agg | 0.03 | 0.22 | 2.46 | 0.91 | 7.68E-03 |
p-value adjusted tor age, sex, smoking, hypertension, dyshpidemia, and diabetes - from haplo.glm
Coeff = estimated regression coefficient.
Note: e^coeff = odds ratio of this haplotype compared to the reference (ref) haplotype
Haplotypes with a frequency < 10 were grouped as ‘Rare Haplotypes’
Note that each haplotype was compared to the most common haplotype as noted by (ref) for each gene, however only haplotypes with p ≤ 0.0125 are presented in this table. Full results are in Supplementary Table S3.