ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.7088del (p.Lys2363fs) (rs876658512)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000216898 SCV000273859 pathogenic Hereditary cancer-predisposing syndrome 2015-02-02 criteria provided, single submitter clinical testing
Molecular Genetics Department,Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology RCV000223734 SCV000267593 pathogenic Ataxia-telangiectasia syndrome no assertion criteria provided research

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