ClinVar Miner

Submissions for variant NM_001349884.2(DRAM2):c.98_99del (p.Leu33fs)

dbSNP: rs2101085885
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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 Human Genetics, University of Leipzig Medical Center RCV001728030 SCV001976412 likely pathogenic Cone-rod dystrophy 21 2021-09-23 criteria provided, single submitter clinical testing

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