ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.1585G>A (p.Val529Ile)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004764705 SCV005374329 uncertain significance Polycystic kidney disease, adult type 2024-09-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV004764705 SCV005638417 likely benign Polycystic kidney disease, adult type 2024-03-16 criteria provided, single submitter clinical testing

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