ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.1134A>G (p.Leu378=)

dbSNP: rs2138059118
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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 RCV001483491 SCV001687883 likely benign Immunodeficiency 67 2022-02-05 criteria provided, single submitter clinical testing

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