ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.8549C>T (p.Ser2850Leu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005014133 SCV005640876 uncertain significance Polycystic kidney disease, adult type 2024-06-20 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005014133 SCV005912137 uncertain significance Polycystic kidney disease, adult type 2021-11-24 criteria provided, single submitter clinical testing

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