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
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs772527880
AGFG1
2 227531108 missense variant G/A snv 4.0E-06 1
rs764987358
ANGPT1
1.000 0.160 8 107347040 missense variant C/A snv 8.0E-06 1.4E-05 2
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs7118900
ANKK1
11 113396099 missense variant G/A snv 0.25 0.25 1
rs1803274
BCHE
0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
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
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
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
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
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
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249