| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial hyperthyroidism due to mutations in TSH receptor +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial gestational hyperthyroidism | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Familial gestational hyperthyroidism | |
| | | Single nucleotide variant (missense variant) | Familial hyperthyroidism due to mutations in TSH receptor +2 more | |
| | | Single nucleotide variant (missense variant) | Familial gestational hyperthyroidism +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial gestational hyperthyroidism | |
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