ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.561T>C (p.Tyr187=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003639472 SCV004385958 likely benign Inflammatory bowel disease 25 2023-06-03 criteria provided, single submitter clinical testing

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