ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.641A>C (p.His214Pro)

dbSNP: rs949664612
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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 RCV001919632 SCV002193995 uncertain significance Inflammatory bowel disease 25 2021-08-30 criteria provided, single submitter clinical testing

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