ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.9926-9C>G

gnomAD frequency: 0.00002  dbSNP: rs772804757
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002544466 SCV001079338 likely benign Chédiak-Higashi syndrome 2024-06-05 criteria provided, single submitter clinical testing

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