ClinVar Miner

Submissions for variant NM_004798.4(KIF3B):c.1481del (p.Gln494fs)

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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 RCV003326223 SCV004032317 likely benign Retinitis pigmentosa 89 2023-09-04 criteria provided, single submitter clinical testing

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