ClinVar Miner

Submissions for variant NM_000130.5(F5):c.3768A>G (p.Thr1256=)

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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 RCV003764295 SCV004529707 likely benign Congenital factor V deficiency 2023-05-12 criteria provided, single submitter clinical testing

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