ClinVar Miner

List of variants reported as uncertain significance for Intellectual disability, autosomal recessive 46 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001543.5(NDST1):c.1360C>T (p.Arg454Cys)	rs150009231	0.00011
NM_001543.5(NDST1):c.1690G>C (p.Val564Leu)	rs774976739	0.00006
NM_001543.5(NDST1):c.2401A>T (p.Thr801Ser)	rs760333260

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