ClinVar Miner

Submissions for variant NM_000572.3(IL10):c.165+20G>A

gnomAD frequency: 0.00001  dbSNP: rs749899175
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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 RCV001489284 SCV001693823 likely benign Inflammatory bowel disease 2022-06-27 criteria provided, single submitter clinical testing

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