| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | |
| | | Microsatellite (inframe_deletion) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 +2 more | |
| | | Deletion (frameshift variant) | Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset +2 more | |
| | | Deletion (frameshift variant) | Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | |
| | | Single nucleotide variant (missense variant) | Paget disease of bone 3 +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene