ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.2312A>G (p.Lys771Arg) (rs61747277)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000147933 SCV000195426 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
GeneDx RCV000147933 SCV000521956 benign not specified 2016-04-12 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Athena Diagnostics Inc RCV000714192 SCV000844879 benign not provided 2018-06-12 criteria provided, single submitter clinical testing
Invitae RCV000714192 SCV001094129 benign not provided 2019-02-14 criteria provided, single submitter clinical testing

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