TABLE 4.
Bivariate multipoint LODeq scores ⩾ 1.9 and test for pleiotropy and coincident linkage
Cytogenetic Position | Closest Marker(s) | Trait | Data Set | LODeq Score (1 Degree of Freedom) | Covariates a | Complete Pleiotropy b | Coincident Linkage b |
---|---|---|---|---|---|---|---|
6p21-p12 | D6S1610-D6S257 | TC-LDL | Samoa | 2.13 c | A, A2, STC, A•SLDL, A2•S, DLDL | 0.500 | 9.8 × 10−4 |
6p21-p12 | D6S1610-D6S257 | TC-LDL | Samoa | 2.25 c | A, A2, S, A•SLDL, A2•S, DLDL, BLDL | 0.500 | 8.1 × 10−16 |
7q34-q35 | D7S661 | TC-LDL | American Samoa | 2.62 | A, A2, STC, CTC,P | 0.020 | 0.002 |
12p12 | D12S1617 | TC-HDL | Combined | 2.17 c | ATC, A2 TC, S, A2•STC, C, PTC, DHDL, EHDL, MHDL, BHDL | ||
12q21 | D12S351 | TC-LDL | American Samoa | 3.38 | A, A2, STC, CTC, P | 0.235 | 5.0 × 10−5 |
12q21 | D12S346 | TC-LDL | Samoa | 2.05 c | A, A2, S, A•SLDL, A2•S, DLDL, BLDL | 0.500 | 7.3 × 10−4 |
12q23 | D12S78 | TC-TG | Combined | 2.58 c | A, A2, S, A2•S, CTC, PTC, DTG, MTG, BTG | 0.028 | 0.625 |
12q24 | D12S1723 | TC-TG | Combined | 2.26 c | A, A2, S, A2•S, CTC, PTC, DTG, MTG, BTG | ||
12q24 | D12S1723 | TC-HDL | Combined | 3.22 c | A, A2, S, A2•STC, C, PTC, DHDL, EHDL, MHDL | 0.008 | 0.017 |
12q24 | D12S1723 | TC-HDL | Combined | 3.00 c | ATC, A2 TC, S, A2•STC, C, PTC, DHDL, EHDL, MHDL, BHDL | N.A. | N.A. |
19p13-q12 | D19S226-D19S414 | TC-LDL | American Samoa | 2.14 | A, A2, STC, CTC, P | 0.395 | 0.001 |
Covariates included in the polygenic model. Subscripts indicate trait-specific covariates.
P value for test of complete pleiotropy (ρq constrained to 1 or −1) and no coincident linkage (ρq constrained to 0) for the maximum LODeq per chromosome. N.A. indicates that convergence failure occurred in SOLAR.
The corrected LOD score (LODmtc) can be calculated by subtracting 0.3 from the uncorrected LOD score shown. LODeq ⩾ 3 is indicated in boldface.