| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Deletion (frameshift variant) | Hypothyroidism due to TSH receptor mutations +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial hyperthyroidism due to mutations in TSH receptor +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypothyroidism due to TSH receptor mutations +2 more | |
| | | Deletion (frameshift variant) | Familial hyperthyroidism due to mutations in TSH receptor +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene