ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.822C>T (p.Leu274=)

dbSNP: rs755330743
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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 RCV002114145 SCV002440853 likely benign Immunodeficiency 67 2022-07-12 criteria provided, single submitter clinical testing

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