ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.12003+1G>T

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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 RCV005019885 SCV005641203 pathogenic Polycystic kidney disease, adult type 2024-04-15 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005365369 SCV005913961 pathogenic Autosomal dominant polycystic kidney disease 2021-08-09 criteria provided, single submitter clinical testing

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