ORMDL3 and asthma: Finally, we searched for whole exome variant sets for variants in ORMDL3 (mutations observed in CD and asthma) under four models: autosomal dominant with affected parental members (model #1), autosomal recessive with affected parental members (model #2), autosomal dominant with mycobacterial susceptible members (model #5), and autosomal recessive with mycobacterial susceptible members (model #6).