ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.318A>G (p.Ala106=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004807813 SCV005430179 likely benign Retinoblastoma 2024-04-25 criteria provided, single submitter clinical testing

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