ClinVar Miner

Submissions for variant NM_018669.6(WDR4):c.138G>A (p.Lys46=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003080852 SCV003486793 benign not provided 2024-01-12 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003080852 SCV004811361 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing WDR4: BP4, BP7

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