List of variants reported as pathogenic for syndromic intellectual disability by Wilkie Group, Clinical Genetics Lab, WIMM, University of Oxford

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
GRCh38/hg38 19q13.2(chr19:41987984-42252574)x1
GRCh38/hg38 19q13.2(chr19:42198610-42249880)x1
NC_000019.10:g.41983952_42247520del

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