ClinVar Miner

Submissions for variant NC_000013.10:g.(32890665_32893213)_(32893463_32899212)del

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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 RCV000508133 SCV000605718 pathogenic Breast-ovarian cancer, familial, susceptibility to, 2 2015-07-01 criteria provided, single submitter clinical testing Heterozygous deletion of exon 3

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