ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.1452C>A (p.Ser484Arg)

dbSNP: rs144437378
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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 RCV001308425 SCV001497874 uncertain significance Immunodeficiency 39 2021-08-26 criteria provided, single submitter clinical testing

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