ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.138C>T (p.Asp46=)

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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 RCV002570112 SCV002936785 likely benign Hereditary antithrombin deficiency 2025-01-29 criteria provided, single submitter clinical testing

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