ClinVar Miner

Submissions for variant NM_001346022.3(USP45):c.7del (p.Arg2_Val3insTer)

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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 RCV004814368 SCV005070055 uncertain significance Retinal dystrophy 2022-01-01 no assertion criteria provided clinical testing

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