Table 3.
Haplotype analyses for Lp(a) and CAAD.
| Trait | SNPs | High risk haplotypes(s)* | Frequency | Lp(a) β or CAAD OR | P-value (Lp(a) % variance)† |
|---|---|---|---|---|---|
| Lp(a) | rs3798221/rs10455872 | GA | 0.017 | 1.8 | 1.3 × 10−76 (21%) |
| AG | 0.076 | 1.8 | |||
| Lp(a) | rs6919346/rs3798221/rs10455872 | GGA | 0.017 | 2.1 | 5.0 × 10−82 (23%) |
| GAG | 0.075 | 2.1 | |||
| GAA | 0.75 | 0.42 | |||
| Lp(a) | rs6919346/rs3798220/rs10455872/rs2295368‡ | GAAA | 0.34 | 0.62 | 4.1 × 10−12 (25%) |
| Lp(a) | rs6919346/rs3798220/rs3798221/rs10455872/rs2295368‡ | GACAA | 0.27 | 0.94 | 8.3 × 10−18 (25%) |
| CAAD | rs6919346/rs10455872 | GG | 0.075 | 2.0 | 0.020 |
| CAAD | rs3123629/rs6919346/rs10455872 | AGG | 0.066 | 2.1 | 0.054 |
Haplotype analyses were performed using covariates as described in Methods.
Haplotypes among the set tested with the largest β for Lp(a) or OR for CAAD.
P-values are for the global test of no difference between haplotypes versus any differences and are Bonferroni corrected for the number of haplotypes tested.
Conditional on the major allele (AA) background of rs3798220 and rs10455872.