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Table 3 Rare-variant association tests for genes associated with ciliopathies and subsets

From: Deleterious genetic variants in ciliopathy genes increase risk of ritodrine-induced cardiac and pulmonary side effects

Database Gene list (No. of genes) Bonferroni corrected P Reference
Burden SKAT SKAT-O
Invitae Ciliopathies (102) 1.00000 1.00000 1.00000 [26]
Joubert and Meckel-Gruber Syndromes (JBTMKS; 30) 0.39528 0.10536 0.19548 [26]
GHR Joubert Syndrome (JBTS; 11) 0.09908 0.05076 0.08020 [27]
Meckel Syndrome (MKS; 8) 1.00000 1.00000 1.00000 [28]
  1. GHR Genetics home references, SKAT sequence kernel association test