ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.1125+14A>G

gnomAD frequency: 0.00004  dbSNP: rs941148757
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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 RCV001462172 SCV001666085 likely benign Immunodeficiency 67 2022-11-08 criteria provided, single submitter clinical testing

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