ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.5744C>T (p.Ser1915Leu)

dbSNP: rs760842136
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Total submissions: 1
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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 RCV003989230 SCV004805789 likely benign Polycystic kidney disease, adult type 2024-03-29 criteria provided, single submitter clinical testing

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