ClinVar Miner

Submissions for variant NM_022154.5(SLC39A8):c.[97G>A;1004G>C];[c.610G>T]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Metabolic Research Unit,Children's University Hospital Muenster RCV000203267 SCV000256231 pathogenic SLC39A8 deficiency 2015-11-03 criteria provided, single submitter research

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