ClinVar Miner

Submissions for variant GRCh37/hg19 Xp22.32(chrX:5073112-5578094)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 Goettingen RCV001250260 SCV001424562 uncertain significance Intellectual disability 2019-06-27 no assertion criteria provided clinical testing

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