Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17110451 12 71930054 downstream gene variant A/G snv 0.12 1
rs11819869
AMBRA1
1.000 0.040 11 46539130 intron variant C/T snv 0.27 2
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
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
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs806379
CNR1
1.000 0.040 6 88151548 intron variant A/C;T snv 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs10078866
DRD1
1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 2
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs2044081
GABRB1
1.000 0.080 4 47216323 intron variant C/T snv 0.14 2
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3