ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.390+7C>T

gnomAD frequency: 0.00016  dbSNP: rs759572399
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000420020 SCV000515258 likely benign not specified 2016-01-20 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.
Genetic Services Laboratory, University of Chicago RCV000420020 SCV002065938 likely benign not specified 2019-07-09 criteria provided, single submitter clinical testing
Invitae RCV002061570 SCV002347098 likely benign not provided 2023-09-19 criteria provided, single submitter clinical testing

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