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
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1805055
HTR2A
0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 3
rs6305
HTR2A
0.882 0.040 13 46892487 synonymous variant G/A snv 1.8E-02 1.7E-02 3
rs147347002
DRD2
1.000 11 113416879 synonymous variant G/A snv 1.9E-04 6.6E-04 1
rs762199332
SLC6A3
1.000 5 1432601 synonymous variant G/A snv 4.0E-06 1