Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs245914
CHN2 ; CPVL
1.000 0.040 7 29178543 intron variant G/A;T snv 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25 4
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs12196860
COL21A1
1.000 0.040 6 56085576 intron variant G/A snv 0.15 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs1341402
DAOA-AS1
1.000 0.040 13 105463160 intron variant T/C snv 0.16 2
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs778294
DAOA ; DAOA-AS1
0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs3738401
DISC1 ; TSNAX-DISC1
0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 4
rs751229
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231632793 intron variant A/G;T snv 2
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11