ClinVar Miner

Submissions for variant NM_001080442.3(SLC38A8):c.789C>T (p.Leu263=)

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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 RCV003552439 SCV004264376 likely benign not provided 2023-05-17 criteria provided, single submitter clinical testing

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