ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.2694A>C (p.Ala898=) (rs142357713)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000251657 SCV000305710 benign not specified criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000251657 SCV000592748 benign not specified 2016-09-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000576584 SCV000604709 benign Polycystic kidney disease, adult type 2018-09-25 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576584 SCV000677402 benign Polycystic kidney disease, adult type 2017-06-09 criteria provided, single submitter clinical testing

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