ClinVar Miner

Submissions for variant NC_000013.10:g.(32944695_32945092)_(32945238_32950806)dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Medical Genetics,Oslo University Hospital RCV000507308 SCV000605720 likely pathogenic Breast-ovarian cancer, familial 2 2016-12-01 criteria provided, single submitter clinical testing Heterozygous duplication of exon 20

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