ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.2739+17C>A

dbSNP: rs144527765
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001567084 SCV001790711 likely benign not provided 2020-07-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001567084 SCV002408076 benign not provided 2023-12-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243306 SCV002514923 benign Microcephaly 2, primary, autosomal recessive, with or without cortical malformations 2021-12-05 criteria provided, single submitter clinical testing

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