ClinVar Miner

Submissions for variant NM_000104.3(CYP1B1):c.622_623GT[2] (p.Cys209fs) (rs104894980)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratoire de Génétique et de Physiologie Neuroendocrinienne, Faculté des Sciences RCV000082863 SCV000109655 not provided Glaucoma 3, primary congenital, A no assertion provided not provided

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