ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.888T>C (p.Ser296=)

dbSNP: rs2082965544
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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 RCV001458421 SCV001662244 likely benign Inflammatory bowel disease 25 2019-09-03 criteria provided, single submitter clinical testing

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