ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.4689-7T>C

dbSNP: rs1572256602
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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 RCV003635935 SCV001107469 likely benign Chédiak-Higashi syndrome 2023-11-24 criteria provided, single submitter clinical testing

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