| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Neuropathy, hereditary motor and sensory, type VIc, with optic atrophy +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
Click to view in NCBI Gene