ClinVar Miner

Submissions for variant NM_052945.4(TNFRSF13C):c.288G>C (p.Val96=)

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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 RCV002725575 SCV002998856 likely benign Immunodeficiency, common variable, 4 2022-09-13 criteria provided, single submitter clinical testing

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