ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.12602_12635del (p.Leu4201fs)

dbSNP: rs2544578238
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV003441160 SCV004167612 uncertain significance Polycystic kidney disease, adult type 2022-09-19 no assertion criteria provided clinical testing

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