ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.941+18A>G

gnomAD frequency: 0.00683  dbSNP: rs11182261
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001518284 SCV001726950 benign Immunodeficiency 67 2024-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707644 SCV005230559 benign not provided criteria provided, single submitter not provided

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