ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.1836G>A (p.Leu612=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003414973 SCV004126160 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing LYST: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV003523174 SCV004278631 likely benign Chédiak-Higashi syndrome 2023-10-17 criteria provided, single submitter clinical testing

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