Table 2.

Association of variants in SNCA-3’UTR with DLB and PD

Rs Number	Variant Type	Chr. location	Alleles minor/ major	Normal N=101 MAF	DLB N=77 MAF	PD N=70 MAF	DLB OR (95% CI)	PD OR (95% CI)	DLB p value	PD p value
rs1045722	SNP	4:90,645,671	T/A	0.095	0.084	0.085	1.62 (0.70–4.12)	1.11 (0.52– 2.45)	0.264	0.786
rs3857053	SNP	4:90,645,674	A/G	0.095	0.084	0.085	1.59 (0.68–4.02)	1.08 (0.50– 2.41)	0.292	0.835
rs356165	SNP	4:90,646,886	C/T	0.409	0.350	0.343	1.41 (0.88–2.27)	1.25 (0.78– 1.99)	0.149	0.353
rs145304567	SNP	4:90,647,702	A/C	0.020	0.032	0.000	1.69 (0.38–7.51)	-	0.475	0.052
rs10716074	SNP	4:90,647,278	T/C	0.005	0.000	0.000	-	-	0.502	0.564
rs777296100	SSR	4:90,646,470	<20/ 21; 22+	0.090	0.060	0.079	1.18 (1.00–1.41)	1.00 (0.87– 1.17)	0.048	0.947
DEL ATTT	deletion	4:90,647,199	-/ATTT	0.000	0.013	0.014	-	-	0.143	0.166

SNP, single nucleotide polymorphism; SSR, simple sequence repeat; Chr. location based on GRCh37/hg19; N, total number of subjects; MAF, minor allele frequency; Bold P value, indicates significant association