ClinVar Miner

Submissions for variant NM_201253.3(CRB1):c.2298G>A (p.Trp766Ter)

dbSNP: rs1664656299
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Molecular Genetics, University of Zurich RCV001352964 SCV001548037 likely pathogenic CRB1-related maculopathy 2021-01-30 criteria provided, single submitter clinical testing

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