ClinVar Miner

Submissions for variant NM_058216.3:c.(705+1_706-1)_(1131+1_?)del

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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 RCV001823041 SCV002072574 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2022-01-27 criteria provided, single submitter clinical testing _x000D_ Criteria applied: PVS1_STR, PS4_SUP, PM2_SUP

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