ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.596-16C>T (rs62310565)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000247344 SCV000303539 benign not specified criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000247344 SCV000592876 benign not specified 2016-07-27 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000999973 SCV000604827 benign Polycystic kidney disease 2 2018-09-11 criteria provided, single submitter clinical testing

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