ClinVar Miner

Submissions for variant NM_000321.2(RB1):c.1707A>G (p.Leu569=) (rs3092895)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000562366 SCV000674700 likely benign Hereditary cancer-predisposing syndrome 2015-11-24 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000658678 SCV000780463 uncertain significance not provided 2018-02-28 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000397463 SCV000384550 likely benign Retinoblastoma 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000397463 SCV000562097 benign Retinoblastoma 2018-01-12 criteria provided, single submitter clinical testing

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