ClinVar Miner

Submissions for variant NM_000516.7(GNAS):c.312+17T>C

gnomAD frequency: 0.00022  dbSNP: rs78999525
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002131404 SCV002452937 likely benign not provided 2023-12-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002508103 SCV002798469 likely benign McCune-Albright syndrome; Pseudohypoparathyroidism type 1C; Pseudohypoparathyroidism type 1B; Pseudopseudohypoparathyroidism; Progressive osseous heteroplasia; Pituitary adenoma 3, multiple types; ACTH-independent macronodular adrenal hyperplasia 1; Pseudohypoparathyroidism type I A 2021-08-16 criteria provided, single submitter clinical testing

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