Association statistics for the 12 candidate nsSNPs.

For each nsSNP, clinical phenotypes were constructed using diagnosis codes that closely approximated the phenotype descriptions in the OMIM and KO mouse databases. Shown are the subject counts and results of exact logistic regression analyses comparing minor allele homozygotes to matched common allele homozygotes. The common allele homozygotes were matched for age, race, gender and data set.