ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.882T>A (p.Gly294=)

gnomAD frequency: 0.00001  dbSNP: rs1941467982
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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 RCV002152483 SCV002413209 likely benign Immunodeficiency 67 2022-09-01 criteria provided, single submitter clinical testing

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