ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.594G>A (p.Arg198=)

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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 RCV003639320 SCV004554238 likely benign Inflammatory bowel disease 25 2023-03-14 criteria provided, single submitter clinical testing

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