Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs1959536
TRIM9
1.000 0.040 14 50980053 intron variant T/G snv 9.7E-02 2
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4