ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.504_510del (p.Pro167_Trp168insTer)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003333393 SCV004040887 likely pathogenic Somatotroph adenoma 2023-03-29 criteria provided, single submitter clinical testing

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