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 |