ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.*616del

dbSNP: rs5843596
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000372654 SCV000435594 uncertain significance Inflammatory bowel disease 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694631 SCV005195113 uncertain significance not provided criteria provided, single submitter not provided

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