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
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2296972
HTR2A-AS1 ; HTR2A
0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs200889048 0.882 0.120 3 74928276 intergenic variant C/- del 3
rs12490016
LINC00880 ; LINC00881
0.882 0.120 3 157121142 intron variant G/C snv 4.6E-02 3
rs1630623
TMC1
0.882 0.120 9 72725323 intron variant A/G snv 0.29 3
rs1950038 0.925 0.080 2 183579642 regulatory region variant T/C snv 0.71 2
rs73057489 0.925 0.080 12 17370820 regulatory region variant A/C snv 3.9E-02 2
rs7337127 0.925 0.080 13 104623579 intergenic variant C/A;T snv 2
rs6006893
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44858015 intron variant C/T snv 0.15 2
rs726170
ARHGAP8 ; PRR5-ARHGAP8
0.925 0.080 22 44855931 intron variant C/T snv 0.15 2
rs17810023
BCKDHB
0.925 0.080 6 80443056 non coding transcript exon variant C/T snv 1.7E-02 2
rs7904579
CUBN
0.925 0.080 10 17089754 intron variant G/A;C snv 2
rs111940429
LINC01789
0.925 0.080 2 107366232 intron variant C/A;T snv 2