ClinVar Miner

Submissions for variant GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)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 RCV001801194 SCV002047406 pathogenic Specific learning disability 2021-08-18 criteria provided, single submitter clinical testing

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