ClinVar Miner

Submissions for variant NM_000572.3(IL10):c.297G>A (p.Glu99=)

gnomAD frequency: 0.00001  dbSNP: rs1220388430
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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 RCV001403822 SCV001605707 likely benign Inflammatory bowel disease 2019-02-07 criteria provided, single submitter clinical testing

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