Related gene-specific medical variations for Gene (Select 6487) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2436495	NM_006279.5(ST3GAL3):c.-30-12556T>G	ST3GAL3, ST3GAL3-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2436494	NM_006279.5(ST3GAL3):c.209+5G>A	ST3GAL3	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2436493	NM_006279.5(ST3GAL3):c.-31+9864G>A	ST3GAL3, ST3GAL3-AS1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1255027	NM_006279.5(ST3GAL3):c.1039-288C>A	LOC112590792, ST3GAL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1213739	NM_006279.5(ST3GAL3):c.1019G>A (p.Arg340His)	ST3GAL3 (R247H +8 more)	Single nucleotide variant (missense variant +2 more)	Developmental and epileptic encephalopathy, 15	GUncertain significance
Select item 1098663	NM_006279.5(ST3GAL3):c.-31+9631T>C	ST3GAL3, ST3GAL3-AS1	Single nucleotide variant (intron variant)	Developmental and epileptic encephalopathy, 15	GUncertain significance

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