Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1439050
NTRK2
0.925 0.080 9 84673278 intron variant G/A;T snv 2
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5
rs2268115
GRIN2B
1.000 0.040 12 13716791 intron variant G/A;T snv 1
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs3757
DGCR8 ; TRMT2A
0.851 0.160 22 20111808 3 prime UTR variant G/A snv 0.21 5
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs594242
HTR2A
1.000 0.040 13 46883917 intron variant C/A;G snv 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs636832
AGO1
0.790 0.400 1 35897874 intron variant G/A snv 0.23 8