List of variants in gene NDST1 reported as uncertain significance for Intellectual disability, autosomal recessive 46

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001543.5(NDST1):c.239G>A (p.Arg80His)	rs145390254	0.00145
NM_001543.5(NDST1):c.334C>T (p.Arg112Cys)	rs138962514	0.00036
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.389G>A (p.Arg130His)	rs148227466	0.00005
NM_001543.5(NDST1):c.730C>T (p.Arg244Cys)	rs375092472	0.00004
NM_001543.5(NDST1):c.1831G>A (p.Gly611Ser)	rs606231459	0.00001
NM_001543.5(NDST1):c.388C>T (p.Arg130Cys)	rs746465319	0.00001
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.2401A>T (p.Thr801Ser)	rs760333260
NM_001543.5(NDST1):c.2468G>C (p.Gly823Ala)	rs1755738807
NM_001543.5(NDST1):c.2623C>T (p.Arg875Ter)
NM_001543.5(NDST1):c.340G>T (p.Glu114Ter)	rs1085307082
NM_001543.5(NDST1):c.39C>G (p.His13Gln)	rs777877507
NM_001543.5(NDST1):c.985C>T (p.Arg329Cys)

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