"Athena Diagnostics"[submitter] AND "STX1B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 586687	NM_052874.5(STX1B):c.840A>G (p.Ser280=)	STX1B	Single nucleotide variant (synonymous variant)	Generalized epilepsy with febrile seizures plus, type 9 +3 more	GBenign
Select item 542095	NM_052874.5(STX1B):c.837G>A (p.Ala279=)	STX1B	Single nucleotide variant (synonymous variant)	Generalized epilepsy with febrile seizures plus, type 9 +2 more	GBenign/Likely benign
Select item 586686	NM_052874.5(STX1B):c.786+7G>A	STX1B	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 475339	NM_052874.5(STX1B):c.538-5C>G	STX1B	Single nucleotide variant (intron variant)	Inborn genetic diseases +2 more	GBenign
Select item 586685	NM_052874.5(STX1B):c.538-7A>G	STX1B	Single nucleotide variant (intron variant)	Generalized epilepsy with febrile seizures plus, type 9 +3 more	GBenign
Select item 475338	NM_052874.5(STX1B):c.105+10C>T	STX1B	Single nucleotide variant (intron variant)	Generalized epilepsy with febrile seizures plus, type 9 +1 more	GBenign/Likely benign

ClinVar