| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (no sequence alteration) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Primary hyperparathyroidism | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | Multiple endocrine neoplasia +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
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