ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1197T>C (p.Asp399=)

gnomAD frequency: 0.00008  dbSNP: rs34400047
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 RCV002079068 SCV002426126 likely benign Inflammatory bowel disease 28 2023-06-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003222394 SCV003916787 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing IL10RA: BP4, BP7

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