ClinVar Miner

Submissions for variant NM_052945.4(TNFRSF13C):c.137-41_137-19dup

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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 RCV003612443 SCV004553324 likely benign Immunodeficiency, common variable, 4 2023-03-01 criteria provided, single submitter clinical testing

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