ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.10306C>T (p.Gln3436Ter)

dbSNP: rs2151726823
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003446858 SCV004171862 likely pathogenic Polycystic kidney disease, adult type criteria provided, single submitter clinical testing
Laboratory of Gastroenterology and Hepatology, Radboud University Medical Center RCV001844991 SCV001876924 pathogenic Autosomal dominant polycystic kidney disease 2021-09-01 no assertion criteria provided research

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