C4693694[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 167650	NM_006922.4(SCN3A):c.2547A>C (p.Val849=)	SCN3A	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 586501	NM_006922.4(SCN3A):c.2031A>T (p.Thr677=)	SCN3A	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 95445	NM_006922.4(SCN3A):c.1441C>T (p.Leu481=)	SCN3A	Single nucleotide variant (synonymous variant)	Developmental and epileptic encephalopathy, 62 +3 more	GBenign
Select item 1241883	NM_006922.4(SCN3A):c.1381-34G>A	SCN3A	Single nucleotide variant (intron variant)	Epilepsy, familial focal, with variable foci 4 +3 more	GBenign
Select item 1169487	NM_006922.4(SCN3A):c.968-20G>T	SCN3A	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 1221351	NM_006922.4(SCN3A):c.695-46A>G	SCN3A	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 586504	NM_006922.4(SCN3A):c.602+9C>T	SCN3A	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 95444	NM_006922.4(SCN3A):c.127_129del (p.Asn43del)	SCN3A (N43del)	Deletion (inframe_deletion)	not provided +3 more	GBenign

ClinVar