ClinVar Miner

Submissions for variant NM_001006658.3(CR2):c.2323+18A>G

dbSNP: rs2102307081
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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 RCV001467454 SCV001671478 likely benign Immunodeficiency, common variable, 7 2022-09-01 criteria provided, single submitter clinical testing

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