List of variants reported as pathogenic for autism spectrum disorder by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 15q11.2-13.1(chr15:23810397-29213787)
GRCh37/hg19 8p23.1-21.2(chr8:12580104-25947329)
GRCh37/hg19 8p23.3-23.1(chr8:194617-6816918)
GRCh37/hg19 Xp22.31(chrX:6488721-8097511)

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