ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.1855C>T (p.Arg619Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002595961 SCV003499898 benign LAMA2-related muscular dystrophy 2022-05-18 criteria provided, single submitter clinical testing

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