Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs2193352 0.790 0.080 10 99586852 intergenic variant A/G snv 0.15 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs283415
ADH1C ; ADH1B
0.925 0.080 4 99349450 intron variant C/T snv 0.64 2
rs4147542
ADH1C ; ADH1B
0.882 0.160 4 99347396 intron variant T/C snv 0.33 3
rs3811802
ADH1B
0.925 0.080 4 99323064 intron variant A/C;G;T snv 2
rs4147536
ADH1B
0.925 0.080 4 99317955 non coding transcript exon variant A/C snv 0.71 2
rs34405347 0.776 0.080 9 98917470 regulatory region variant T/C;G snv 10
rs1407508 0.790 0.080 9 98882256 regulatory region variant T/C snv 4.1E-02 9
rs145364999
CHD1
0.776 0.080 5 98870378 intron variant T/A snv 1.9E-03 10
rs2732875
SHROOM2
0.790 0.080 X 9795858 intron variant C/G;T snv 9
rs5934683
GPR143
0.790 0.080 X 9783434 intron variant T/C snv 0.50 9
rs11692435
ACTR1B
0.790 0.080 2 97658891 missense variant G/A snv 7.0E-02 6.7E-02 10
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs756363791
OGG1
0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs67376798
DPYD
0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05 9
rs1724120
ASTL ; DUSP2
0.925 0.080 2 96143592 3 prime UTR variant T/C snv 0.53 2
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs1799853
CYP2C9
0.763 0.320 10 94942290 missense variant C/T snv 9.2E-02 8.9E-02 11
rs9409565
LOC107987100
0.790 0.080 9 94488752 intron variant C/G;T snv 9
rs119490107
FSBP ; RAD54B
0.925 0.080 8 94399540 missense variant C/A snv 2.8E-05 2
rs13149359 0.776 0.080 4 94017467 intergenic variant C/A snv 0.29 10