ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.1233+15del

dbSNP: rs373693641
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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 RCV000192527 SCV000249442 likely benign not specified 2013-06-05 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000299793 SCV000411628 uncertain significance Primary Microcephaly 2 With or Without Cortical Malformations 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001512685 SCV001720144 benign not provided 2024-12-21 criteria provided, single submitter clinical testing

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