ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.501C>T (p.Asn167=)

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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 RCV005086568 SCV005721326 likely benign Hereditary antithrombin deficiency 2024-05-13 criteria provided, single submitter clinical testing

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