Genotypes were ultimately determined for 251 subjects. The total additive genetic variance (heritability, h2) and its standard error were estimated for the CD, ASPD, ASPD/CD phenotypes using SOLAR (http://www.sfbr.org/solar/). Two approaches to estimating heritability were used for the three traits. In the first approach the trait was modeled as a latent normally distributed variable with a threshold above which an individual is considered “affected”. Using a second approach, the same trait was modeled as if it was a normally distributed variable. In this case heritability is higher for the trait modeled as if it was a normally distributed variable. These methods can occasionally give very dissimilar results presumably because of factors related to convergence. In this analysis it was required that both methodologies provide support for heritability prior to linkage analyses. Variance component estimate methods were used to calculate LOD scores using SOLAR v2.0.4 (Almasy and Blangero, 1998) Genhunter 2 (Kruglyak et al., 1996) and Merlin (http://www.sph.umich.edu/csg/abecasis/Merlin/) with similar results. Results are presented for SOLAR. Simulation analysis was used to estimate empirical LOD scores and make appropriate genome wide adjustments
