ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.885A>C (p.Ala295=)

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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 RCV002794805 SCV003024454 likely benign Immunodeficiency 67 2023-07-12 criteria provided, single submitter clinical testing

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