ClinVar Miner

Submissions for variant NM_000322.5:c.(581+1_582-1)_(828+1_829-1)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 RCV004817694 SCV005070936 pathogenic Retinal dystrophy 2020-01-01 criteria provided, single submitter clinical testing

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