| | | Deletion (frameshift variant +3 more) | McCune-Albright syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudopseudohypoparathyroidism +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +9 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +9 more | |
| | | Deletion (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (intron variant) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Progressive osseous heteroplasia +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (genic upstream transcript variant +3 more) | not provided +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +9 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | GNAS-related condition +8 more | |
| | | Single nucleotide variant (nonsense +1 more) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +8 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | GNAS-related condition +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | GNAS-related condition +8 more | |
| | | Single nucleotide variant (splice donor variant) | McCune-Albright syndrome | |
| | | Duplication | Cushing syndrome +7 more | |
| | | Single nucleotide variant (genic upstream transcript variant +3 more) | Pseudohypoparathyroidism type 1C +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Pseudohypoparathyroidism type 1C +7 more | |
| | | Duplication (frameshift variant +1 more) | Pseudohypoparathyroidism type I A +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Progressive osseous heteroplasia +11 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (5 prime UTR variant +1 more) | McCune-Albright syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pseudohypoparathyroidism type 1B +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pseudohypoparathyroidism type 1C +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | McCune-Albright syndrome +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | ACTH-independent macronodular adrenal hyperplasia 1 +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | McCune-Albright syndrome +10 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pseudohypoparathyroidism +10 more | |
| | | Single nucleotide variant (genic upstream transcript variant +3 more) | not provided +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | McCune-Albright syndrome +9 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | McCune-Albright syndrome +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | GNAS-related condition +9 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | GNAS-related condition +9 more | |
| | | Microsatellite (inframe_deletion +1 more) | McCune-Albright syndrome | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Progressive osseous heteroplasia +9 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | Cushing syndrome +7 more | |
| | | Single nucleotide variant (intron variant +1 more) | Cushing syndrome +16 more | |
| | | Single nucleotide variant (missense variant +1 more) | McCune-Albright syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm | |
| | | Single nucleotide variant (missense variant +1 more) | McCune-Albright syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Neoplasm +10 more | |
| | | Single nucleotide variant (nonsense +1 more) | GNAS-related condition +11 more | |
| | | Single nucleotide variant (genic upstream transcript variant +3 more) | GNAS-related condition +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | Pituitary adenoma 3, multiple types +8 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pituitary adenoma 3, multiple types +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pituitary adenoma 3, multiple types +8 more | |
| | | Single nucleotide variant (missense variant +2 more) | GNAS-related condition +9 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pituitary adenoma 3, multiple types +8 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pseudohypoparathyroidism type 1B +8 more | |
| | | Single nucleotide variant (missense variant +1 more) | McCune-Albright syndrome | |
| | | Deletion (frameshift variant +1 more) | Pseudohypoparathyroidism type 1C +13 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pituitary adenoma 3, multiple types | |
| | | Single nucleotide variant (missense variant +1 more) | Pseudohypoparathyroidism type I A +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pituitary adenoma 3, multiple types +8 more | GPathogenic/Likely pathogenic |