ClinVar Miner

Submissions for variant NM_000506.5(F2):c.1437C>T (p.His479=)

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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 RCV003627259 SCV004524312 likely benign Congenital prothrombin deficiency 2023-03-13 criteria provided, single submitter clinical testing

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