| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062906, LOC130062907
+222 more | Copy number loss | See cases | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Copy number gain | See cases | |
Click to view in NCBI Gene