ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.112G>A (p.Gly38Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003990106 SCV004806413 uncertain significance Merosin deficient congenital muscular dystrophy 2024-03-25 criteria provided, single submitter clinical testing

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