ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.2424G>A (p.Pro808=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002606329 SCV003499285 likely benign not provided 2023-01-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002606329 SCV004123949 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing LAMC2: BP4, BP7

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