| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | TMX2-CTNND1, TMX2 (L103fs +4 more) | Deletion (frameshift variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | TMX2, TMX2-CTNND1 (R114W +4 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene