ClinVar Miner

Submissions for variant NM_000506.5(F2):c.789C>T (p.Arg263=)

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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 RCV003515511 SCV004368401 likely benign Congenital prothrombin deficiency 2023-06-09 criteria provided, single submitter clinical testing

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