ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.999C>T (p.Pro333=)

gnomAD frequency: 0.00001  dbSNP: rs570350055
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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 RCV001412823 SCV001614922 likely benign Inflammatory bowel disease 28 2019-10-30 criteria provided, single submitter clinical testing

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