ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.5922+10A>G

dbSNP: rs375422713
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000629240 SCV000750163 likely benign Chédiak-Higashi syndrome 2024-01-31 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004689816 SCV005184705 likely benign not specified 2024-05-30 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702531 SCV001931527 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001702531 SCV001974459 likely benign not provided no assertion criteria provided clinical testing

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