List of variants in gene ST3GAL3 reported as likely pathogenic for epilepsy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006279.5(ST3GAL3):c.166+1G>A	rs148531289	0.00002
NC_000001.10:g.(?_44257753)_(44365419_?)dup
NM_006279.5(ST3GAL3):c.118+1G>A	rs2154091891
NM_006279.5(ST3GAL3):c.167-2A>G
NM_006279.5(ST3GAL3):c.167-2A>T
NM_006279.5(ST3GAL3):c.210-1G>C
NM_006279.5(ST3GAL3):c.397+2T>C	rs200255759
NM_006279.5(ST3GAL3):c.558-19_562del
NM_006279.5(ST3GAL3):c.891+1G>T	rs2082857900
NM_006279.5(ST3GAL3):c.891+2T>G

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