ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.123G>A (p.Glu41=)

gnomAD frequency: 0.00013  dbSNP: rs140495014
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000937678 SCV001083468 likely benign Inflammatory bowel disease 25 2023-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003438601 SCV004153111 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing IL10RB: BP4, BP7

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