ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.67+10C>T

gnomAD frequency: 0.00002  dbSNP: rs55721363
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000268478 SCV000344043 uncertain significance not provided 2016-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001470596 SCV001674692 likely benign Inflammatory bowel disease 28 2023-12-13 criteria provided, single submitter clinical testing

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