ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.6927C>T (p.Gly2309=) (rs189277711)

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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 RCV000247949 SCV000305769 benign not specified criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000247949 SCV000592796 benign not specified 2016-10-21 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755358 SCV000604713 benign Polycystic kidney disease, adult type 2019-03-24 criteria provided, single submitter clinical testing

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