ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.215C>T (p.Thr72Met)

gnomAD frequency: 0.00019  dbSNP: rs148466782
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000916193 SCV001061426 likely benign Inflammatory bowel disease 25 2024-01-04 criteria provided, single submitter clinical testing
Baylor Genetics RCV000916193 SCV001526144 uncertain significance Inflammatory bowel disease 25 2018-11-03 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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