ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1158C>G (p.Thr386=)

gnomAD frequency: 0.00180  dbSNP: rs4252290
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Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000647213 SCV000769002 benign Inflammatory bowel disease 28 2024-01-19 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002060758 SCV002497178 likely benign not provided 2022-03-01 criteria provided, single submitter clinical testing IL10RA: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV002060758 SCV005211744 likely benign not provided criteria provided, single submitter not provided

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