ClinVar Miner

Submissions for variant NM_000628.5(IL10RB):c.147C>T (p.Asn49=)

dbSNP: rs781729452
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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 RCV001481108 SCV001685443 likely benign Inflammatory bowel disease 25 2021-02-26 criteria provided, single submitter clinical testing

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