ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.172G>A (p.Glu58Lys)

gnomAD frequency: 0.00004  dbSNP: rs572945136
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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 RCV000908434 SCV001053196 likely benign Inflammatory bowel disease 28 2023-10-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704305 SCV005211689 likely benign not provided criteria provided, single submitter not provided

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