Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs8042149
RORA
0.882 0.160 15 60832754 intron variant T/G snv 0.44 3