ClinVar Miner

Submissions for variant NM_000130.5(F5):c.3582C>T (p.Thr1194=)

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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 RCV003841411 SCV004692859 likely benign Congenital factor V deficiency 2023-08-28 criteria provided, single submitter clinical testing

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