ClinVar Miner

Submissions for variant NM_005560.6(LAMA5):c.9078G>A (p.Ala3026=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV005402456 SCV006060261 uncertain significance not provided 2024-10-24 criteria provided, single submitter clinical testing In silico analysis supports a deleterious effect on splicing; Has not been previously published as pathogenic or benign to our knowledge

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