List of variants reported as uncertain significance for autism, susceptiblity to by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.236G>T (p.Gly79Val)	rs150900180	0.00001
NM_001170629.2(CHD8):c.1030G>A (p.Val344Met)	rs753886912
NM_001170629.2(CHD8):c.1880C>G (p.Pro627Arg)	rs1888694098
NM_001170629.2(CHD8):c.410G>A (p.Gly137Asp)	rs752288417
NM_001170629.2(CHD8):c.5749G>A (p.Gly1917Ser)	rs1887663294
NM_006593.4(TBR1):c.1816C>A (p.Pro606Thr)	rs1684280120

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