Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
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
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs3808607 0.716 0.400 8 58500365 upstream gene variant G/T snv 0.55 16
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs1234314 0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs12762303 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs572527200 0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs59439148 0.925 0.160 10 45374100 upstream gene variant GGGGGCGGGGGCGGGGGCGGGGGC/-;GGGGGC;GGGGGCGGGGGC;GGGGGCGGGGGCGGGGGC;GGGGGCGGGGGCGGGGGCGGGGGCGGGGGC;GGGGGCGGGGGCGGGGGCGGGGGCGGGGGCGGGGGC;GGGGGCGGGGGCGGGGGCGGGGGCGGGGGCGGGGGCGGGGGC delins 0.16 4
rs10733113 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 3
rs1361600 0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs7213516 0.882 0.080 17 63474189 upstream gene variant G/A snv 5.7E-02 3
rs7913948 1.000 0.080 10 45373441 upstream gene variant G/A snv 0.17 3
rs1324694 0.925 0.120 10 100186688 upstream gene variant C/T snv 7.8E-02 2
rs2001846 1.000 0.080 8 125466208 upstream gene variant T/A;C snv 2
rs10176176 1.000 0.080 2 85534925 upstream gene variant A/T snv 0.54 1
rs13210554 1.000 0.080 6 46736602 upstream gene variant C/T snv 0.20 1