ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.301C>A (p.Arg101=)

dbSNP: rs368287711
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001458344 SCV001662166 likely benign Inflammatory bowel disease 28 2023-08-24 criteria provided, single submitter clinical testing
GeneDx RCV001773750 SCV002001424 uncertain significance not provided 2024-03-24 criteria provided, single submitter clinical testing In silico analysis supports that this variant does not alter splicing; Has not been previously published as pathogenic or benign to our knowledge

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