ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.236G>A (p.Arg79Lys)

dbSNP: rs760219197
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001319722 SCV001510480 likely benign LAMA2-related muscular dystrophy 2024-09-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706089 SCV005225234 likely benign not provided criteria provided, single submitter not provided
Mayo Clinic Laboratories, Mayo Clinic RCV004706089 SCV005407977 uncertain significance not provided 2024-01-19 criteria provided, single submitter clinical testing BP5

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