Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs2020936
SLC6A4
0.776 0.160 17 30223796 intron variant G/A;C snv 10
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 4
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs4259397 0.925 0.040 8 92354062 upstream gene variant G/A;T snv 2
rs4858253 0.925 0.040 3 20687599 intron variant C/T snv 0.33 2
rs74760947 0.925 0.040 8 34495092 intergenic variant A/G snv 3.1E-02 2
rs797267 0.925 0.040 12 89373460 intron variant A/G snv 0.28 2
rs2875907
CADM2
0.925 0.040 3 85469430 intron variant A/G;T snv 2
rs806374
CNR1
0.925 0.080 6 88147601 intron variant T/C snv 0.37 2
rs1476535
FOXP2
0.925 0.040 7 114430980 intron variant C/G;T snv 2
rs2189012
FOXP2
0.925 0.040 7 114571857 intron variant G/A snv 0.73 2
rs56319043
KDM4A-AS1 ; ST3GAL3 ; KDM4A
0.925 0.040 1 43705540 intron variant C/T snv 0.17 2
rs139868495
LINC01288
0.925 0.040 8 34805452 intron variant C/T snv 3.1E-02 2