ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.7436-17T>G

dbSNP: rs81002829
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003237426 SCV002010331 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA2) RCV000113758 SCV000147085 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 2 2003-12-23 no assertion criteria provided clinical testing

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