List of variants in gene SLC35A2 reported as uncertain significance for Inborn genetic diseases

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005660.3(SLC35A2):c.169G>A (p.Ala57Thr)	rs151120284	0.00011
NM_005660.3(SLC35A2):c.1099C>A (p.Gln367Lys)	rs1452748811	0.00002
NM_005660.3(SLC35A2):c.584T>G (p.Leu195Arg)	rs1569511154	0.00001
NM_005660.3(SLC35A2):c.826C>T (p.Leu276Phe)	rs782737391	0.00001
NM_005660.3(SLC35A2):c.1030G>A (p.Ala344Thr)	rs369861178
NM_005660.3(SLC35A2):c.1030G>T (p.Ala344Ser)
NM_005660.3(SLC35A2):c.26C>T (p.Ser9Phe)
NM_005660.3(SLC35A2):c.335C>G (p.Thr112Arg)	rs1557043139
NM_005660.3(SLC35A2):c.35C>G (p.Ala12Gly)	rs1557044100
NM_005660.3(SLC35A2):c.700C>T (p.Arg234Cys)	rs2063481027
NM_005660.3(SLC35A2):c.818G>A (p.Gly273Asp)	rs1557042798

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