ClinVar Miner

Submissions for variant NM_001009944.3:c.(9201+1_9398-1)_(10050+1_10051-1)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, University of Leipzig Medical Center RCV004759582 SCV005368268 uncertain significance Polycystic kidney disease, adult type 2024-08-08 criteria provided, single submitter clinical testing Criteria applied: PVS1_MOD,PM2;PP4

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