ClinVar Miner

Submissions for variant NM_001289125.3(IFNAR2):c.158_160del (p.Ser53del)

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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 RCV003992135 SCV004812108 likely pathogenic Immunodeficiency 45 2024-03-11 criteria provided, single submitter clinical testing

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