ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.762G>A (p.Leu254=)

gnomAD frequency: 0.00002  dbSNP: rs1033025102
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000791494 SCV000930746 likely benign Inflammatory bowel disease 28 2024-01-06 criteria provided, single submitter clinical testing

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