ClinVar Miner

Submissions for variant NM_000506.5(F2):c.1347C>A (p.Ile449=)

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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 RCV003628581 SCV004453792 likely benign Congenital prothrombin deficiency 2023-04-08 criteria provided, single submitter clinical testing

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