ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.11723T>C (p.Leu3908Pro)

dbSNP: rs2151688569
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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, University of Leipzig Medical Center RCV001374662 SCV001571430 pathogenic Polycystic kidney disease, adult type 2021-04-19 criteria provided, single submitter clinical testing

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