ClinVar Miner

Submissions for variant NM_017875.4(SLC25A38):c.-161G>A (rs528990278)

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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 RCV000345376 SCV000444261 uncertain significance Hereditary sideroblastic anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000391690 SCV000444262 uncertain significance Refractory anemia with ringed sideroblasts (clinical) 2016-06-14 criteria provided, single submitter clinical testing

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