| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (5 prime UTR variant +2 more) | Constitutional megaloblastic anemia with severe neurologic disease +3 more | |
| | | Insertion (5 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Microsatellite (5 prime UTR variant +2 more) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | MSH3-related condition +3 more | |
Click to view in NCBI Gene