ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.3756G>A (p.Gln1252=)

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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 RCV002812018 SCV003211233 likely benign Achondrogenesis, type IA 2022-06-15 criteria provided, single submitter clinical testing

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