ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.4527G>A (p.Ser1509=)

gnomAD frequency: 0.00006  dbSNP: rs374574870
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502266 SCV000597966 likely benign not specified 2017-06-22 criteria provided, single submitter clinical testing
Invitae RCV002056887 SCV002382467 likely benign not provided 2023-06-29 criteria provided, single submitter clinical testing

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