Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750802
PSEN1
0.851 0.080 14 73219144 missense variant T/G snv 7
rs63751032
PSEN1
0.851 0.080 14 73219156 missense variant T/A;G snv 7
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 5
rs74315414
PRNP
0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs121918304
FBXO7
0.925 0.080 22 32498453 stop gained C/A;T snv 4.0E-06; 4.0E-06 4
rs368134308
PRKN
0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs63750444
PSEN1
0.882 0.080 14 73192745 missense variant G/A snv 4
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4
rs137852538
PGK1
0.925 0.080 X 78117385 missense variant A/T snv 3
rs1426868527
MIR6084 ; PINK1
1 20633841 missense variant G/A;T snv 3
rs1555727942
NOTCH3 ; MIR6795
0.925 0.160 19 15180807 missense variant G/A snv 3
rs267604921
MAPT
0.925 0.160 17 45993953 missense variant C/A;G;T snv 6.3E-05; 2.5E-04; 5.3E-06 3
rs369634041
PRKN
6 162262647 missense variant C/A;T snv 4.0E-06; 2.0E-05 3
rs63751165
MAPT
0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs74315360
PINK1
0.925 0.040 1 20638104 missense variant C/A snv 3
rs774457232
EIF4G1
0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs781442277
PTRHD1 ; CENPO ; LOC105369164
1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs1057518882
CYTB ; ND5 ; ND6
MT 14598 missense variant T/C snv 2
rs1239756674
MAOA
1.000 0.040 X 43743818 synonymous variant G/A snv 2
rs139548132
WARS2 ; WARS2-AS1
1.000 1 119140608 missense variant A/C;G;T snv 3.2E-03; 1.6E-05; 4.0E-06 2
rs2421947
DNM3-IT1 ; DNM3
1.000 0.040 1 171863954 intron variant C/G;T snv 2