ClinVar Miner

Submissions for variant NM_000130.5(F5):c.4113C>T (p.Ser1371=)

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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 RCV005192516 SCV005819514 likely benign Congenital factor V deficiency 2024-06-19 criteria provided, single submitter clinical testing

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