ClinVar Miner

Submissions for variant NM_017875.4(SLC25A38):c.*472G>T (rs141567816)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000342953 SCV000444295 likely benign Hereditary sideroblastic anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000376052 SCV000444296 likely benign Refractory anemia with ringed sideroblasts (clinical) 2016-06-14 criteria provided, single submitter clinical testing

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