List of variants reported as uncertain significance for Intellectual disability, autosomal dominant 45 by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001386298.1(CIC):c.4273G>A (p.Gly1425Arg)	rs777753069	0.00002
NM_001386298.1(CIC):c.3928T>C (p.Phe1310Leu)	rs752892028	0.00001
NM_001386298.1(CIC):c.2653G>A (p.Ala885Thr)
NM_001386298.1(CIC):c.6484G>T (p.Ala2162Ser)	rs910167566

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