ClinVar Miner

Submissions for variant NM_000506.5(F2):c.1137G>A (p.Val379=)

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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 RCV005187876 SCV005820335 likely benign Congenital prothrombin deficiency 2025-01-03 criteria provided, single submitter clinical testing

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