Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs7124442
BDNF-AS ; BDNF
0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
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
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs3760138
AANAT
0.807 0.160 17 76467027 intron variant G/A;T snv 6
rs6195
NR3C1
0.807 0.120 5 143399752 missense variant T/A;C snv 6
rs8150
AANAT ; RHBDF2
0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 6
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 5
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5