Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs3495
BCHE
0.925 0.160 3 165773193 3 prime UTR variant C/A;T snv 3
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs9450898
CNR1
0.925 0.160 6 88154344 intron variant C/T snv 0.21 3
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2