ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.954C>T (p.Asp318=)

gnomAD frequency: 0.00005  dbSNP: rs759956227
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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 RCV000925034 SCV001070562 likely benign Inflammatory bowel disease 28 2023-11-24 criteria provided, single submitter clinical testing

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