ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.1374A>G (p.Thr458=)

dbSNP: rs2138089009
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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 RCV002097523 SCV002384259 likely benign Immunodeficiency 67 2023-07-17 criteria provided, single submitter clinical testing

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