ClinVar Miner

Submissions for variant NM_001006658.3(CR2):c.2238T>C (p.Asp746=)

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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 RCV003646518 SCV004503866 likely benign Immunodeficiency, common variable, 7 2023-11-29 criteria provided, single submitter clinical testing

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