ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.10092dup (p.Leu3365fs)

dbSNP: rs1567165997
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000735665 SCV002810938 pathogenic Polycystic kidney disease, adult type 2021-11-13 criteria provided, single submitter clinical testing
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000735665 SCV000863806 pathogenic Polycystic kidney disease, adult type 2018-01-23 no assertion criteria provided clinical testing

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