Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752834812
NR3C1
0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs772651364
NR3C1
0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 5
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2144025
ESR1
0.925 0.080 6 151986571 intron variant T/A;C snv 4
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1553510492
TBR1
2 161419040 missense variant A/G snv 4
rs72653772
ABCC6
0.807 0.320 16 16190246 missense variant C/T snv 8.4E-05 1.1E-04 16
rs121918805
LOC102724058 ; SCN1A-AS1 ; SCN1A
0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs587784177
NSD1
0.790 0.280 5 177283827 missense variant G/A snv 20
rs3915512
DLG1 ; MIR4797
1.000 0.040 3 197295369 intron variant A/G;T snv 3
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2279709
SLC18A1
0.882 0.120 8 20178722 intron variant T/G snv 0.51 5
rs35369693
AVPR1B
1 206116696 missense variant C/G;T snv 4.3E-02 2
rs142441643
SDHA
0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 15
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs200754713
PSEN2
1 226888954 missense variant A/G snv 4.0E-06; 4.0E-06 2
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs773758385
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694162 missense variant C/T snv 1.0E-04 3.5E-05 3
rs373288445
DISC1 ; TSNAX-DISC1
0.925 0.080 1 231694534 missense variant C/T snv 5.6E-05 4.2E-05 3