Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004212
NRXN3
14 78714883 synonymous variant C/G;T snv 8.0E-06; 0.15 2
rs10078866
DRD1
1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs11178999
TPH2
12 71939790 intron variant G/A snv 0.27 1
rs1131691771
PHIP ; IRAK1BP1
0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs1135402761
SYT1
0.827 0.320 12 79448958 missense variant T/C snv 11
rs11617488
LOC107984582
13 21619823 intergenic variant A/G snv 0.27 1
rs11624704
NRXN3
1.000 0.080 14 78319734 intron variant A/C snv 0.13 3
rs11819869
AMBRA1
1.000 0.040 11 46539130 intron variant C/T snv 0.27 2
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs144900171
SYT1
0.925 12 79448968 missense variant C/G;T snv 1.3E-04 6.2E-04 5
rs1455858
LOC349160 ; CHRM2
0.925 0.080 7 136946956 intron variant T/C snv 0.69 3
rs1473473
TPH2
0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 4
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs1554210073
PHIP
0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs1555565492
RAI1
0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs1562150844
PHIP
0.790 0.280 6 78982908 frameshift variant CTTT/- delins 14
rs1565922388
SYT1
0.925 12 79353599 missense variant T/A snv 5
rs1565922395
SYT1
0.925 12 79353602 missense variant A/G snv 5
rs1565962725
SYT1
0.925 12 79448953 missense variant C/A snv 5
rs17110451 12 71930054 downstream gene variant A/G snv 0.12 1