ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.231A>C (p.Thr77=)

gnomAD frequency: 0.00001  dbSNP: rs772817746
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001484100 SCV001688508 likely benign Immunodeficiency 67 2022-08-23 criteria provided, single submitter clinical testing

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