ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.676C>T (p.Leu226=)

dbSNP: rs2137961403
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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 RCV002157638 SCV002336065 likely benign Immunodeficiency 67 2021-03-20 criteria provided, single submitter clinical testing

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