ClinVar Miner

Submissions for variant GRCh37/hg19 7p22.1(chr7:5096876-5569338)x1

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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 RCV001801207 SCV002047419 pathogenic Astigmatism; Autistic behavior; Myopia; Impaired social interactions; Aplasia/Hypoplasia of the inner ear 2020-10-22 criteria provided, single submitter clinical testing

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