ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.90G>A (p.Pro30=)

gnomAD frequency: 0.00006  dbSNP: rs747872407
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 RCV000533341 SCV000648409 likely benign Inflammatory bowel disease 28 2023-09-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704083 SCV005211678 likely benign not provided criteria provided, single submitter not provided

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