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
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs139455627
TSPEAR
0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs74315442
CSTB
0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs864309483
ADCY5
0.851 0.080 3 123352464 missense variant G/A snv 9
rs1064794533
GNAO1
0.882 0.080 16 56336846 missense variant G/A snv 4
rs1345423
GRIN2A
1.000 0.080 16 10154207 intron variant G/A;C;T snv 1
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs752513525
NDUFA13
0.882 0.120 19 19526257 missense variant G/A;T snv 2.4E-05 3
rs113994152
TSEN54
0.790 0.160 17 75522000 missense variant G/T snv 9.0E-04 9.0E-04 11
rs393795
SLC6A3
0.851 0.160 5 1428399 intron variant G/T snv 0.28 4
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7