ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.2883G>A (p.Lys961=)

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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 RCV003614763 SCV004453678 likely benign Achondrogenesis, type IA 2024-02-05 criteria provided, single submitter clinical testing

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