"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SYNJ1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1673649	NM_203446.3(SYNJ1):c.3697+12T>G	SYNJ1	Single nucleotide variant (intron variant)	Early-onset Parkinson disease 20 +1 more	GLikely benign
Select item 478326	NM_203446.3(SYNJ1):c.6G>A (p.Ala2=)	SYNJ1	Single nucleotide variant (synonymous variant)	Developmental and epileptic encephalopathy, 53 +2 more	GBenign/Likely benign