ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1635T>G (p.Leu545=)

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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 RCV003852544 SCV004663200 likely benign Inflammatory bowel disease 28 2022-12-24 criteria provided, single submitter clinical testing

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