ClinVar Miner

Submissions for variant NM_001006658.3(CR2):c.1168C>T (p.Gln390Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005017422 SCV005640498 likely pathogenic Systemic lupus erythematosus, susceptibility to, 9; Immunodeficiency, common variable, 7 2024-02-09 criteria provided, single submitter clinical testing

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