ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.766+20_766+21del

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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 RCV003016730 SCV003319693 likely benign Immunodeficiency 39 2022-08-09 criteria provided, single submitter clinical testing

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