ClinVar Miner

Submissions for variant NM_015330.6(SPECC1L):c.2259C>G (p.Leu753=)

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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 RCV003714378 SCV004488498 likely benign not provided 2022-12-31 criteria provided, single submitter clinical testing

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