ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.413A>G (p.Asp138Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
School of Medicine, Universitat de Girona RCV003140300 SCV003804967 uncertain significance Danon disease no assertion criteria provided research

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