Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs760761 0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
rs2619522 0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs4648308 0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27 5