| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC105378448, LOC107195252
+245 more | Copy number loss | See cases | |
| | LOC130004555, LOC130004556
+375 more | Copy number loss | See cases | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases +2 more | |
| | | Duplication (frameshift variant) | not provided | |
Click to view in NCBI Gene