Disease: Depressive disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs78162420
TPH2
0.882 0.120 12 71941600 missense variant C/A snv 2.1E-03 7.1E-04 4
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1876828
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs6267
MIR4761 ; COMT
0.827 0.200 22 19962740 missense variant G/A;T snv 4.8E-05; 1.4E-02 9
rs9722
S100B
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs885479
MC1R
0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83