ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.123A>G (p.Lys41=)

gnomAD frequency: 0.00006  dbSNP: rs551138584
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001407829 SCV001609811 likely benign Immunodeficiency 67 2022-07-19 criteria provided, single submitter clinical testing

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