ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1716T>C (p.Ser572=)

dbSNP: rs1256548482
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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 RCV002135855 SCV002453154 likely benign Inflammatory bowel disease 28 2023-11-10 criteria provided, single submitter clinical testing

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