ClinVar Miner

Submissions for variant NM_207361.6(FREM2):c.1815A>G (p.Leu605=)

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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 RCV003696756 SCV004458307 likely benign not provided 2023-04-17 criteria provided, single submitter clinical testing

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