ClinVar Miner

Submissions for variant NM_000130.5(F5):c.2136T>A (p.Arg712=)

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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 RCV003873883 SCV004680156 likely benign Congenital factor V deficiency 2022-12-10 criteria provided, single submitter clinical testing

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