Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs702764
OPRK1
0.925 0.120 8 53229597 synonymous variant T/C;G snv 0.17; 8.0E-06 4
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs3495
BCHE
0.925 0.160 3 165773193 3 prime UTR variant C/A;T snv 3
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs9450898
CNR1
0.925 0.160 6 88154344 intron variant C/T snv 0.21 3
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs764987358
ANGPT1
1.000 0.160 8 107347040 missense variant C/A snv 8.0E-06 1.4E-05 2
rs3025684
CREBBP
1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 2
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs2377339
NCK2
2 105840835 intron variant A/G snv 4.8E-02 2
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs17664708
NRG1
1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs772527880
AGFG1
2 227531108 missense variant G/A snv 4.0E-06 1