ClinVar Miner

Submissions for variant NM_017875.4(SLC25A38):c.227_236del (p.Lys76fs)

dbSNP: rs2125578633
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mark Fleming Laboratory, Boston Children's Hospital RCV001526377 SCV001736700 pathogenic Sideroblastic anemia 2 2021-06-01 criteria provided, single submitter research

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