ClinVar Miner

Submissions for variant NM_001558.4(IL10RA):c.1038A>G (p.Arg346=)

dbSNP: rs2134995931
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001506843 SCV001711781 likely benign Inflammatory bowel disease 28 2019-11-05 criteria provided, single submitter clinical testing

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