ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.876T>C (p.Tyr292=)

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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 RCV002863057 SCV003225134 likely benign Hereditary antithrombin deficiency 2021-12-02 criteria provided, single submitter clinical testing

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