| | | Single nucleotide variant (missense variant) | Multiple endocrine neoplasia, type 2 +8 more | |
| | | Single nucleotide variant (missense variant) | Multiple endocrine neoplasia, type 2 +2 more | |
| | | Single nucleotide variant (missense variant) | RET-related condition +10 more | |
| | | Single nucleotide variant (intron variant) | Multiple endocrine neoplasia, type 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Hirschsprung disease, susceptibility to, 1 +8 more | |
| | | Single nucleotide variant (missense variant) | Multiple endocrine neoplasia, type 2 +5 more | |
| | | Single nucleotide variant (missense variant) | Ependymoma | |
| | | Single nucleotide variant (missense variant +1 more) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA +1 more | |
| | | Single nucleotide variant (missense variant) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA +2 more | |
| | | Single nucleotide variant (missense variant) | RET-related condition +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Multiple endocrine neoplasia, type 2 +7 more | |
| | | Single nucleotide variant (missense variant) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Pheochromocytoma +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RET-related condition +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial medullary thyroid carcinoma +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial medullary thyroid carcinoma +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Multiple endocrine neoplasia, type 2 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | RET-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | RET-related condition +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA +4 more | |
| | | Single nucleotide variant (missense variant) | Hirschsprung disease, susceptibility to, 1 +5 more | |
| | | Single nucleotide variant (missense variant) | Hirschsprung disease, susceptibility to, 1 +8 more | GConflicting classifications of pathogenicity |