ClinVar Miner

Submissions for variant NM_032415.7(CARD11):c.358+1_358+9delinsAACATC

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen RCV004723652 SCV005328345 likely pathogenic Immunodeficiency 11b with atopic dermatitis 2024-09-25 criteria provided, single submitter clinical testing

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