ClinVar Miner

Submissions for variant NM_004385.5(VCAN):c.4004G>T (p.Gly1335Val)

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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 RCV004759603 SCV005368309 uncertain significance Wagner syndrome 2024-08-20 criteria provided, single submitter clinical testing Criteria applied: PM2, PP3

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