ClinVar Miner

Submissions for variant NM_138691.3(TMC1):c.735C>T (p.Asp245=)

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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 RCV003546248 SCV004271170 likely benign not provided 2025-01-24 criteria provided, single submitter clinical testing

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