List of variants reported as uncertain significance for autosomal recessive non-syndromic intellectual disability by Department of Human Genetics, Hannover Medical School

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006618.5(KDM5B):c.4108T>G (p.Leu1370Val)	rs200000027	0.00021
NM_005883.3(APC2):c.1778C>T (p.Ser593Leu)	rs750829429	0.00005
NM_001160372.4(TRAPPC9):c.1540T>A (p.Cys514Ser)
NM_003619.4(PRSS12):c.359A>C (p.Glu120Ala)
NM_006618.5(KDM5B):c.469A>T (p.Thr157Ser)

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