ClinVar Miner

Submissions for variant NM_198880.3(QRICH1):c.1234del (p.Thr412fs)

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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 RCV003388853 SCV004100694 likely pathogenic Ververi-Brady syndrome 2022-12-19 criteria provided, single submitter clinical testing

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