ClinVar Miner

Submissions for variant NM_025114.4(CEP290):c.41A>G (p.Asp14Gly)

dbSNP: rs2138306044
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DBGen Ocular Genomics RCV001591914 SCV001816073 uncertain significance Leber congenital amaurosis 10 2021-06-02 criteria provided, single submitter clinical testing

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