ClinVar Miner

Submissions for variant NM_001322934.2(NFKB2):c.104-1G>C

dbSNP: rs2061116343
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001262601 SCV001440533 likely pathogenic Immunodeficiency, common variable, 10 2020-10-06 criteria provided, single submitter clinical testing

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