Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs7968585 0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs16861194 0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15 2
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 5
rs2112347 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 5
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3813929 0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs5082 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33