ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.2573C>T (p.Thr858Met)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Royal Melbourne Hospital RCV005250443 SCV005900406 uncertain significance Autosomal dominant polycystic kidney disease 2024-09-08 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005393017 SCV006052512 uncertain significance Polycystic kidney disease, adult type 2022-12-28 criteria provided, single submitter clinical testing

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