ClinVar Miner

Submissions for variant NM_000539.3(RHO):c.778_789del (p.Ala260_Ile263del)

dbSNP: rs2084789357
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genomic Medicine, Manchester, Central Manchester University Hospitals RCV001265159 SCV001443244 uncertain significance Retinitis pigmentosa 4 2020-09-01 criteria provided, single submitter clinical testing

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