Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs864309483
ADCY5
0.851 0.080 3 123352464 missense variant G/A snv 9
rs1563945076
APTX
0.925 0.160 9 32974556 frameshift variant A/- del 4
rs165815
ARVCF
0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72 5
rs267606670
ATP1A3
0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1554389088
CAMK2B
0.807 0.160 7 44243526 missense variant G/A snv 27
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs147484110
CSTB
0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs74315442
CSTB
0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1267306614
DRD3
1.000 0.080 3 114171850 missense variant C/G snv 1
rs1064794533
GNAO1
0.882 0.080 16 56336846 missense variant G/A snv 4
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs1345423
GRIN2A
1.000 0.080 16 10154207 intron variant G/A;C;T snv 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs387907128
LOC112268170 ; PRRT2
0.925 0.080 16 29813850 missense variant C/T snv 4.0E-06 7.0E-06 2
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7