ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1_67+1del

dbSNP: rs2057986431
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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 RCV001352890 SCV001547199 pathogenic Inflammatory bowel disease 28 2021-02-25 no assertion criteria provided clinical testing

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