ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.2857-14T>A

dbSNP: rs535718824
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251196 SCV000304138 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057354 SCV002374714 benign LAMA2-related muscular dystrophy 2024-09-29 criteria provided, single submitter clinical testing

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