List of variants reported as uncertain significance for Schinzel-Giedion syndrome; Intellectual disability, autosomal dominant 29

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_015559.3(SETBP1):c.3802G>A (p.Gly1268Arg)	rs748393505	0.00003
NM_015559.3(SETBP1):c.655C>T (p.His219Tyr)	rs556231993	0.00003
NM_015559.3(SETBP1):c.3632A>G (p.Lys1211Arg)	rs144471715	0.00001
NM_015559.3(SETBP1):c.1058_1059delinsTC (p.Asp353Val)	rs2145095402
NM_015559.3(SETBP1):c.2621ACA[2] (p.Asn876del)	rs755486319
NM_015559.3(SETBP1):c.2903G>A (p.Arg968Lys)
NM_015559.3(SETBP1):c.3022C>G (p.Arg1008Gly)	rs776187085
NM_015559.3(SETBP1):c.3256A>G (p.Met1086Val)
NM_015559.3(SETBP1):c.4572_4578del (p.Pro1525fs)	rs1568058985
NM_015559.3(SETBP1):c.540+1G>A
NM_015559.3(SETBP1):c.540+7390C>T
NM_015559.3(SETBP1):c.540+7438A>G
NM_015559.3(SETBP1):c.812G>A (p.Gly271Glu)	rs749422908

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