| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense +1 more) | Pseudopseudohypoparathyroidism +11 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C | |
| | | Duplication (frameshift variant +1 more) | not provided +8 more | |
| | | Microsatellite (frameshift variant +1 more) | Pseudohypoparathyroidism type 1C | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudohypoparathyroidism +11 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene