ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.3902C>G (p.Pro1301Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002290294 SCV002580265 uncertain significance Polycystic kidney disease, adult type 2021-08-06 criteria provided, single submitter clinical testing

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