ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.1731C>T (p.Thr577=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003613534 SCV004399956 likely benign Achondrogenesis, type IA 2023-10-13 criteria provided, single submitter clinical testing

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