ClinVar Miner

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

dbSNP: rs373693641
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000180555 SCV000233019 benign not specified 2014-11-11 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000392212 SCV000411627 uncertain significance Primary Microcephaly 2 With or Without Cortical Malformations 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001551151 SCV001771595 likely benign not provided 2020-06-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001551151 SCV002406818 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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