Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs852426 0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs62524579 8 142979538 downstream gene variant G/A;C;T snv 4
rs8098380 18 721563 downstream gene variant A/C snv 0.33 4
rs12063100 1 188865413 downstream gene variant G/A;T snv 3
rs12124383 1.000 0.080 1 155946002 downstream gene variant G/A snv 3.7E-03 2
rs3851059 10 80270902 downstream gene variant G/A snv 0.27 2
rs1125226 8 58506952 downstream gene variant C/A snv 0.54 1
rs2093395 6 41187288 downstream gene variant G/C snv 0.29 1
rs275646 3 148745735 downstream gene variant T/C snv 0.95 1
rs35530071 17 7659807 downstream gene variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTTT delins 1
rs834576 6 44238042 downstream gene variant C/A snv 0.16 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
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26