ClinVar Miner

Submissions for variant GRCh37/hg19 Xp11.22(chrX:52923471-53765589)x2

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genetics Laboratory, State University of Rio de Janeiro RCV001270430 SCV001338683 pathogenic Intellectual disability 2020-06-16 criteria provided, single submitter research

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