Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs610932 0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs13227860 1.000 0.040 7 22114836 downstream gene variant G/A snv 0.26 2
rs1879553 0.925 0.040 3 118896616 downstream gene variant A/G snv 7.3E-02 2
rs10506095 1.000 0.040 12 32647193 downstream gene variant C/T snv 4.4E-02 1
rs12921479 1.000 0.040 16 88862799 downstream gene variant T/C snv 0.39 1
rs1296028 1.000 0.040 8 11841238 downstream gene variant A/G snv 0.20 1
rs16938508 1.000 0.040 8 72938577 downstream gene variant A/G snv 0.12 1
rs1775143 1.000 0.040 1 205786422 downstream gene variant C/T snv 0.63 1
rs329648 1.000 0.040 11 133895472 downstream gene variant T/C snv 0.55 1
rs8118008 1.000 0.040 20 3187520 downstream gene variant A/G snv 0.35 1
rs9468199 1.000 0.040 6 27713436 downstream gene variant G/A snv 0.26 1
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1927914 0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14