| | LOC126805952, LOC126805953 +455 more | Copy number loss | See cases | |
| | LOC129388668, LOC129388669 +477 more | Copy number loss | See cases | |
| | LOC129932244, LOC129932245 +1147 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Parathyroid carcinoma +2 more | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Parathyroid carcinoma +2 more | |
| | | Single nucleotide variant | Parathyroid carcinoma +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Parathyroid carcinoma +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism 2 with jaw tumors +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism 2 with jaw tumors +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism 1 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism 2 with jaw tumors +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Duplication (5 prime UTR variant) | Hereditary cancer-predisposing syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Deletion (5 prime UTR variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hyperparathyroidism +3 more | GConflicting classifications of pathogenicity |
| | | Deletion | Parathyroid carcinoma | |
| | | Duplication | Parathyroid carcinoma | |
| | | Deletion | Parathyroid carcinoma | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Duplication (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Duplication (frameshift variant +1 more) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Deletion (frameshift variant +1 more) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant +1 more) | Hyperparathyroidism 2 with jaw tumors | |
| | | Duplication (frameshift variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hyperparathyroidism 2 with jaw tumors +3 more | |
| | | Indel (frameshift variant) | Ossifying fibroma of the jaw | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Duplication (frameshift variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Deletion (inframe_deletion) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | Ossifying fibroma of the jaw | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (nonsense) | Parathyroid carcinoma +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma +1 more | |
| | | Single nucleotide variant (nonsense) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (frameshift variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Hyperparathyroidism 1 +4 more | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Microsatellite (inframe_deletion) | Parathyroid carcinoma | |
| | | Single nucleotide variant (nonsense) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | Parathyroid carcinoma | |
| | | Deletion (frameshift variant) | Cystic parathyroid adenoma | |
| | | Microsatellite (frameshift variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (nonsense) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |
| | | Single nucleotide variant (missense variant) | Parathyroid carcinoma | |