ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.8896G>T (p.Glu2966Ter) (rs773129632)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics,Sultan Qaboos University Hospital, Oman RCV000761501 SCV000891620 uncertain significance Polycystic kidney disease, adult type 2017-12-30 criteria provided, single submitter curation

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