Table 1. Suggestive PD risk non-synonymous variant (p-value < 0.05) within genes known to be involved in familial form of PD.

SNV	Chromosome	Position	Gene	AA subtitution	Allele	MAF (Cases)	MAF (Controls)	Odds Ratio	Pval
rs2302464	4	15709252	BST1	R/Q	A/G	0.018	0.039	0.44	0.042
rs1801334	6	161781225	PARK2	D/N	T/C	0.026	0.046	0.56	0.038
rs33995883	12	40740686	LRRK2	N/D	G/A	0.020	0.010	1.96	0.044
rs2270968	3	182755209	MCCC1	H/P	T/G	0.285	0.240	1.26	0.014