ClinVar Miner

Submissions for variant NM_022154.5(SLC39A8):c.610G>T (rs779241085)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000733882 SCV000861985 uncertain significance not provided 2018-06-26 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000733882 SCV001154211 likely pathogenic not provided 2016-09-01 criteria provided, single submitter clinical testing
OMIM RCV000203248 SCV000258312 pathogenic SLC39A8-CDG 2015-12-03 no assertion criteria provided literature only

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