ClinVar Miner

Submissions for variant NM_000321.2(RB1):c.1156A>G (p.Met386Val) (rs564780653)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000989116 SCV000629268 benign Retinoblastoma 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000570461 SCV000674716 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-30 criteria provided, single submitter clinical testing Insufficient evidence
Mendelics RCV000989116 SCV001139315 likely benign Retinoblastoma 2019-05-28 criteria provided, single submitter clinical testing

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