ClinVar Miner

Submissions for variant NM_000321.2(RB1):c.1914C>A (p.Thr638=) (rs770072166)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000873203 SCV001015157 likely benign Retinoblastoma 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV001013678 SCV001174296 likely benign Hereditary cancer-predisposing syndrome 2019-12-02 criteria provided, single submitter clinical testing In silico models in agreement (benign);Other data supporting benign classification

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