"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 586762	NM_203446.3(SYNJ1):c.186_187insAATACT	SYNJ1	Insertion (inframe_insertion +2 more)	Early-onset Parkinson disease 20 +2 more	GBenign
Select item 586761	NM_203446.3(SYNJ1):c.3721C>T (p.Leu1241=)	SYNJ1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1209924	NM_203446.3(SYNJ1):c.3588+14C>T	SYNJ1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 586760	NM_203446.3(SYNJ1):c.3518-7G>T	SYNJ1	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1168202	NM_203446.3(SYNJ1):c.1201-3A>T	SYNJ1	Single nucleotide variant (intron variant)	Early-onset Parkinson disease 20 +2 more	GBenign
Select item 586758	NM_203446.3(SYNJ1):c.884A>G (p.Lys295Arg)	SYNJ1 (K334R +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign

ClinVar