ClinVar Miner

Submissions for variant NC_000011.10:g.(?_48359351)_(48946475_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo RCV000208722 SCV000172704 uncertain significance Autism spectrum disorder 2012-01-01 no assertion criteria provided research

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