| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion | Neuropathy, hereditary sensory and autonomic, type 1C | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | Neuropathy, hereditary sensory and autonomic, type 1C | |
| | | Single nucleotide variant (intron variant) | not provided | |
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