| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (3 prime UTR variant) | TMED3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMED3-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TMED3-related disorder | |
| | | Copy number loss | not provided | |
Click to view in NCBI Gene