ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.1126-19A>T

gnomAD frequency: 0.00802  dbSNP: rs11182263
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 RCV001512226 SCV001719607 benign Immunodeficiency 67 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707636 SCV005230562 benign not provided criteria provided, single submitter not provided

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