List of variants reported as uncertain significance for autosomal recessive non-syndromic intellectual disability by Daryl Scott Lab, Baylor College of Medicine

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014026.6(DCPS):c.87G>T (p.Glu29Asp)	rs147935593	0.00061
NM_006618.5(KDM5B):c.200C>A (p.Pro67Gln)
NM_017721.5(CC2D1A):c.1276G>A (p.Val426Met)	rs200445152
NM_017721.5(CC2D1A):c.1903A>T (p.Thr635Ser)
NM_017721.5(CC2D1A):c.2365C>T (p.Arg789Trp)

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