ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.657C>T (p.Pro219=)

gnomAD frequency: 0.00001  dbSNP: rs1237354106
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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 RCV001453198 SCV001656882 likely benign Inflammatory bowel disease 25 2020-06-14 criteria provided, single submitter clinical testing

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