Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 2
rs735555
CDK5R1
0.925 0.080 17 32490432 3 prime UTR variant C/T snv 0.30 3
rs35693326
CDKL5 ; RS1
X 18653446 missense variant G/A;T snv 8.5E-03; 5.5E-06 1
rs398122917
CLIC2
0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 5
rs761249181
COL9A1
6 70252139 missense variant C/T snv 1.6E-05 1
rs930549037
COL9A2
1 40301333 missense variant C/T snv 4.4E-05 2.8E-05 1
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs141228574
COQ4
1.000 0.200 9 128332233 missense variant G/C snv 6.3E-03 5.5E-03 2
rs121918368
CRBN ; TRNT1
0.925 0.200 3 3150939 stop gained G/A snv 8.0E-06 7.0E-06 3
rs587777623
DEAF1
0.882 0.120 11 686986 missense variant G/A snv 4.0E-06 8
rs374854258
DGCR2
22 19065049 missense variant G/A snv 2.0E-05 3.5E-05 1
rs749451963
DGCR2
22 19064948 missense variant C/T snv 4.0E-06 1
rs225010
DIO2
1.000 0.200 14 80205936 intron variant C/T snv 0.51 2
rs225012
DIO2
1.000 0.200 14 80204392 intron variant A/C;G snv 0.51 2
rs749457448
DLG3 ; DLG3-AS1
1.000 0.200 X 70452622 start lost A/G snv 2
rs752306
DRD4
0.925 0.200 11 637622 intron variant C/T snv 6.4E-02 4.8E-02 3
rs3758653
DRD4
1.000 0.200 11 636399 upstream gene variant T/C snv 0.20 2
rs1287153074
FOXP1
1.000 0.080 3 70977021 missense variant T/C snv 4.0E-06 7.0E-06 2
rs1294642759
FOXP1
1.000 0.080 3 70959372 missense variant C/T snv 2
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs747138999
GABRA1
1.000 0.040 5 161895753 missense variant G/T snv 2
rs132630328
GK
0.925 0.200 X 30720721 missense variant A/G;T snv 5.4E-06 3
rs1372862248
GPT2
1.000 0.120 16 46926991 missense variant G/A snv 2
rs672601378
GRIN2B ; LOC105369668
0.882 0.040 12 13615149 missense variant C/T snv 4
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13