ClinVar Miner

Submissions for variant GRCh37/hg19 17q21.31(chr17:41199581-41231493)x4

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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 RCV003329541 SCV004036127 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 1 2023-01-05 criteria provided, single submitter clinical testing

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