ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.1593C>T (p.Cys531=)

gnomAD frequency: 0.00060  dbSNP: rs150514010
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000902231 SCV001046643 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000902231 SCV004702230 likely benign not provided 2023-12-01 criteria provided, single submitter clinical testing LAMB1: BP4, BP7
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004782597 SCV005395853 likely benign not specified 2024-09-16 criteria provided, single submitter clinical testing

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