ClinVar Miner

Submissions for variant NM_000321.2(RB1):c.2356C>T (p.Pro786Ser) (rs754507551)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000528489 SCV000629305 likely benign not provided 2019-02-26 criteria provided, single submitter clinical testing
Clinical Genomics Lab,St. Jude Children's Research Hospital RCV000761011 SCV000890926 uncertain significance Medulloblastoma 2016-02-10 no assertion criteria provided clinical testing

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