ClinVar Miner

Submissions for variant NM_000572.3(IL10):c.375C>A (p.Arg125=)

dbSNP: rs755403362
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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 RCV001482986 SCV001687367 likely benign Inflammatory bowel disease 2019-06-05 criteria provided, single submitter clinical testing

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