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
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1803274
BCHE
0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1799972
OPRM1
0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs3495
BCHE
0.925 0.160 3 165773193 3 prime UTR variant C/A;T snv 3
rs2044081
GABRB1
1.000 0.080 4 47216323 intron variant C/T snv 0.14 2
rs2465811
PTPRB
1.000 0.080 12 70596274 missense variant T/A;C snv 0.27; 3.2E-05 1
rs1189608960
PTPRU
1.000 0.080 1 29258684 missense variant G/A snv 4.0E-06 1
rs3278
SLC4A7
1.000 0.080 3 27433860 intron variant G/A snv 0.13 1