ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.3515-7G>A

gnomAD frequency: 0.00006  dbSNP: rs368668756
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000147959 SCV000195452 uncertain significance Microcephaly 2, primary, autosomal recessive, with or without cortical malformations 2013-04-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002514851 SCV002961906 likely benign not provided 2023-09-10 criteria provided, single submitter clinical testing

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