ClinVar Miner

Submissions for variant NM_000321.3(RB1):c.1333-9dup

dbSNP: rs766968771
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000281082 SCV000384545 likely benign Retinoblastoma 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000281082 SCV002478564 benign Retinoblastoma 2024-01-18 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256199 SCV002528289 uncertain significance Hereditary cancer-predisposing syndrome 2021-07-12 criteria provided, single submitter curation

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