ClinVar Miner

Submissions for variant NM_000506.5(F2):c.945C>T (p.Thr315=)

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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 RCV005190862 SCV005822230 likely benign Congenital prothrombin deficiency 2024-05-02 criteria provided, single submitter clinical testing

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