ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.5615T>G (p.Val1872Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Medizinische Genetik Mainz RCV003991364 SCV004808693 uncertain significance Polycystic kidney disease, adult type 2022-10-26 criteria provided, single submitter clinical testing ACMG Criteria: PM2_SUP, PP3, PP4 (ACMG Version 4)

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