ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.5661A>G (p.Glu1887=)

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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 RCV002114907 SCV002444640 likely benign Chédiak-Higashi syndrome 2024-07-01 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004782889 SCV005394037 likely benign not specified 2024-09-04 criteria provided, single submitter clinical testing

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