Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1805502
GRIN2B
0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs7204609
FTO
0.827 0.200 16 53799693 intron variant T/C snv 0.14 6
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 5
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs16917204
BDNF-AS
0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 5
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5