Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750522
PSEN1
0.827 0.120 14 73173644 missense variant G/A;C snv 8
rs542171324
SNCA
0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 6
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs34995376
LRRK2
0.807 0.080 12 40310435 missense variant G/A snv 7.0E-06 7
rs121908683
PLA2G6
0.925 0.080 22 38115667 missense variant G/A snv 9.0E-06 2.1E-05 5
rs3135500
NOD2
0.851 0.160 16 50732975 3 prime UTR variant G/A snv 0.44 5
rs762472005
SACM1L
0.851 0.040 3 45722873 missense variant G/A snv 1.2E-05 7.0E-06 5
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs63750444
PSEN1
0.882 0.080 14 73192745 missense variant G/A snv 4
rs71653619
PARK7
1.000 0.040 1 7970934 missense variant G/A snv 7.9E-03 7.0E-03 4
rs761807915
PRNP
0.925 0.120 20 4699824 missense variant G/A snv 4.0E-06 7.0E-06 4
rs12817488
CCDC62
1.000 0.040 12 122811747 intron variant G/A snv 0.39 3
rs1555727942
NOTCH3 ; MIR6795
0.925 0.160 19 15180807 missense variant G/A snv 3
rs74315356
PINK1-AS ; PINK1
0.925 0.040 1 20649054 stop gained G/A snv 4.0E-06 1.4E-05 3
rs111501952
LRRK2
1.000 0.040 12 40310461 missense variant G/A snv 4.4E-05 7.7E-05 2
rs1239756674
MAOA
1.000 0.040 X 43743818 synonymous variant G/A snv 2
rs757199733
TTN
2 178799505 missense variant G/A snv 8.0E-06 7.0E-06 2
rs45467995
PINK1 ; PINK1-AS
1 20649062 missense variant G/A snv 1
rs758414077
FTL
19 48966681 synonymous variant G/A snv 8.0E-06 2.8E-05 1
rs756677845
PINK1
1 20638074 frameshift variant G/- del 1
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30