ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3674G>A (p.Arg1225His) (rs61743589)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000147965 SCV000195458 benign not specified 2013-02-08 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000348138 SCV000411666 uncertain significance Primary Microcephaly 2 With or Without Cortical Malformations 2016-06-14 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000710285 SCV000616290 benign not provided 2017-11-17 criteria provided, single submitter clinical testing

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