| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary insensitivity to pain with anhidrosis +2 more | |
| | | Deletion (splice acceptor variant) | Hereditary insensitivity to pain with anhidrosis | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary insensitivity to pain with anhidrosis +3 more | GConflicting classifications of pathogenicity |
| | | Insertion (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary insensitivity to pain with anhidrosis | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Hereditary insensitivity to pain with anhidrosis | GPathogenic/Likely pathogenic |
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