List of variants reported as uncertain significance for Intellectual disability, autosomal recessive 46 by Revvity Omics, Revvity

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001543.5(NDST1):c.334C>T (p.Arg112Cys)	rs138962514	0.00036
NM_001543.5(NDST1):c.883G>A (p.Val295Met)	rs747017483	0.00001
NM_001543.5(NDST1):c.2063G>A (p.Arg688Gln)
NM_001543.5(NDST1):c.2272G>A (p.Ala758Thr)
NM_001543.5(NDST1):c.2623C>T (p.Arg875Ter)

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