ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.469-17T>C

gnomAD frequency: 0.00001  dbSNP: rs886037872
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002057273 SCV002357811 likely benign not provided 2024-12-15 criteria provided, single submitter clinical testing
Korbonits Lab, Queen Mary University of London RCV000240417 SCV000298236 uncertain significance Familial isolated pituitary adenoma 2016-08-19 no assertion criteria provided research

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