ClinVar Miner

Submissions for variant NM_001083961.2(WDR62):c.2580C>T (p.Pro860=)

dbSNP: rs886043531
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000397337 SCV000340556 uncertain significance not provided 2016-04-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004725145 SCV005339113 likely benign WDR62-related disorder 2024-06-04 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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