ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.465T>C (p.Asn155=)

gnomAD frequency: 0.00121  dbSNP: rs138883237
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 RCV000645975 SCV000767730 benign Inflammatory bowel disease 25 2024-01-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717700 SCV005307716 benign not provided criteria provided, single submitter not provided

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