ClinVar Miner

Submissions for variant GRCh37/hg19 10q22.3-23.2(chr10:81611360-89264122)x3

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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 RCV003329515 SCV004036100 pathogenic See cases 2022-07-04 criteria provided, single submitter clinical testing

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