ClinVar Miner

Submissions for variant NM_004586.3(RPS6KA3):c.846-13A>G

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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 RCV002592305 SCV003500216 likely benign Coffin-Lowry syndrome; Intellectual disability, X-linked 19 2022-05-06 criteria provided, single submitter clinical testing

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