ClinVar Miner

Submissions for variant NM_016123.4(IRAK4):c.307+8G>C

dbSNP: rs1008518843
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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 RCV001422988 SCV001625554 likely benign Immunodeficiency 67 2021-03-12 criteria provided, single submitter clinical testing

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