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Table 2 Summary of ClinVar data involving SETMAR

From: SETMAR, a case of primate co-opted genes: towards new perspectives

Alterations Nb of involved genes n Clinical significance
Deletions > 20 50 pathogenic
4 to 20 21 pathogenic to likely pathogenic
< 4 15 from likely benign to uncertain significance
SETMAR alone none  
duplications > 20 19 From pathogenic to uncertain significance
4 to 20 4 from pathogenic to uncertain significance
< 4 3 uncertain significance
SETMAR alone none  
  1. Genetic alterations are either deletions or insertions and concerned a variable number of genes (over 20 to SETMAR alone). The number of observed cases is given (n), as well as the clinical relevance