ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.684G>A (p.Arg228=)

dbSNP: rs2134989421
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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 RCV002144450 SCV002470246 likely benign Inflammatory bowel disease 28 2021-04-29 criteria provided, single submitter clinical testing

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