Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 4
rs2514218 0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26 4
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
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
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
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
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249