ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.21C>T (p.Ser7=)

dbSNP: rs923846042
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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 RCV001408882 SCV001610892 likely benign Inflammatory bowel disease 25 2024-04-22 criteria provided, single submitter clinical testing

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