ClinVar Miner

Submissions for variant NM_000081.4(LYST):c.10053G>A (p.Ser3351=)

gnomAD frequency: 0.00023  dbSNP: rs146872810
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001490936 SCV001695511 likely benign Chédiak-Higashi syndrome 2020-07-16 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003994179 SCV004812986 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing

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