ClinVar Miner

Submissions for variant NM_002185.5(IL7R):c.221+1G>A

dbSNP: rs1580851910
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Molecular Medicine, Children’s Hospital of Fudan University RCV001030043 SCV001190564 pathogenic Immunodeficiency 104 2019-05-10 criteria provided, single submitter clinical testing

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