Two susceptibility genes, in linkage disequilibrium with alleles of th
e markers D1G31 and D5G23, have been identified for the disease in the
simulated data set of Problem 1. Here we apply the MASC (marker assoc
iation segregation chi-square) method to model the joint effect of the
se two genes, by testing two-locus models. The model we obtain, that i
s the most parsimonious and that best fits the data, corresponds to a
direct involvement of the alleles D1G31-8 and D5G23-7, with a nonmulti
plicative effect of the two alleles. This was indeed assumed in the tr
ue model used for simulating the data. (C) 1995 Wiley-Liss, Inc.