ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.1188+6T>C

gnomAD frequency: 0.00001  dbSNP: rs372909606
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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 RCV001350174 SCV001544556 uncertain significance Immunodeficiency 67 2021-09-02 criteria provided, single submitter clinical testing

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