Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
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
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs79874540
PSMD1 ; HTR2B
0.925 0.080 2 231123707 stop gained G/A snv 1.5E-03 1.2E-03 4
rs4245146
DRD2
1.000 0.040 11 113447251 intron variant T/C snv 0.49 3
rs594242
HTR2A
1.000 0.040 13 46883917 intron variant C/A;G snv 3
rs279827
GABRA2
4 46332685 splice region variant A/G;T snv 0.44 0.41 2
rs6925
ABHD6
3 58294362 3 prime UTR variant G/A snv 0.53 1