ClinVar Miner

Submissions for variant NM_000313.4(PROS1):c.1866T>C (p.Leu622=)

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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 RCV003642491 SCV004510505 likely benign Thrombophilia due to protein S deficiency, autosomal recessive 2023-04-08 criteria provided, single submitter clinical testing

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