ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.2262dup (p.Pro755fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV004586477 SCV005077850 likely pathogenic Polycystic kidney disease, adult type 2024-06-21 criteria provided, single submitter clinical testing

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