ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.4879C>T (p.Arg1627Trp)

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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 RCV002644020 SCV003512723 likely benign LAMA2-related muscular dystrophy 2024-01-29 criteria provided, single submitter clinical testing
Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University RCV003319243 SCV003932415 uncertain significance Hypertrophic cardiomyopathy 2023-06-01 criteria provided, single submitter clinical testing

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