ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.966G>T (p.Gly322=)

gnomAD frequency: 0.00001  dbSNP: rs780187887
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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 RCV001430786 SCV001633531 likely benign Inflammatory bowel disease 25 2020-05-27 criteria provided, single submitter clinical testing

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