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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs2284411
GRIN2B
1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3
rs429699
SLC6A3
0.925 0.080 5 1409012 intron variant T/C snv 0.96 0.98 3
rs3785143
SLC6A2
1.000 0.040 16 55661194 intron variant C/T snv 8.6E-02 2
rs27048
SLC6A3
1.000 0.040 5 1412530 intron variant C/A;G;T snv 2
rs12861247
STS
1.000 0.040 X 7256158 intron variant G/A snv 7.1E-02 2
rs17268988
STS
1.000 0.040 X 7336440 intron variant C/G snv 0.22 2
rs7984966
HTR2A-AS1 ; HTR2A
13 46855311 intron variant T/A;C snv 1
rs3785157
SLC6A2
16 55695924 intron variant C/T snv 0.26 1