ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.360A>G (p.Val120=)

dbSNP: rs1989246111
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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 RCV002126877 SCV002408558 likely benign Inflammatory bowel disease 25 2021-10-06 criteria provided, single submitter clinical testing

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