ClinVar Miner

Submissions for variant NM_000404.4(GLB1):c.1061T>G (p.Ile354Ser) (rs397515613)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics MedGen RCV000056403 SCV000087512 not provided GM1 gangliosidosis type 2 no assertion provided not provided

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