ClinVar Miner

Submissions for variant NM_001142800.2:c.(1766+1_1767-1)_(2023+1_2024-1)del

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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, Univ. Regensburg, Univ. Regensburg RCV004817314 SCV005070626 pathogenic Retinal dystrophy 2017-01-01 criteria provided, single submitter clinical testing

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