Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs188286943
VPS35
0.776 0.160 16 46662452 missense variant C/T snv 9
rs34015634
LRRK2
0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs774005786
PARK7
0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 8
rs63750522
PSEN1
0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs63750577
PSEN1
0.827 0.120 14 73186881 missense variant C/T snv 8
rs112176450
EIF4G1
0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs34995376
LRRK2
0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
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
rs387907571
DNAJC13
0.827 0.080 3 132477995 missense variant A/G snv 4.2E-06 3.5E-05 6
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs3135500
NOD2
0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5
rs45539432
PINK1-AS ; PINK1
0.851 0.040 1 20649109 stop gained C/T snv 4.0E-05 3.5E-05 5
rs121908683
PLA2G6
0.925 0.080 22 38115667 missense variant G/A snv 9.0E-06 2.1E-05 5
rs74315414
PRNP
0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 5
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 5
rs762472005
SACM1L
0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5
rs201106962
SNCA
0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 5
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 4