ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.7452-4A>C

gnomAD frequency: 0.00016  dbSNP: rs770296949
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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 RCV001516321 SCV001724589 benign LAMA2-related muscular dystrophy 2024-11-03 criteria provided, single submitter clinical testing

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