| SLE (cases) | Controls |
---|
 | Males | Females | Males | Females |
---|
Participants | 9 | 102 | 28 | 84 |
C/C genotype | 7 | 90 | 28 | 74 |
C/T genotype | 2 | 12 | 0 | 10 |
 | S1 (avg) | S2(sum) | S3(genotype) |  |
TD0 (both) | 0.776 | 0.8575 | 0.8575 | Â |
TD1 (only sib pairs) | 0.9263 | 1 | 1 | Â |
TD2 (only triads) | 0.3173 | 0.3173 | 0.3173 | Â |
- We have used 48 multigenerational, multiplex families for our family-based association analysis using the PDT program [19]. The test retains a key property of the "transmission disequilibrium test (TDT)", in that it is valid even when there is population substructure or stratification. The PDT program performs both allele-specific and genotype-specific LD analysis of individual markers. T-test was used to assess the significance of for mean differences in general characteristics between SLE and normal subjects. We did not find a single individual in our pedigrees that presented with a T/T genotype, though the reported T/T genotype in African American population is 3.2%.