Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs2740210 0.827 0.120 20 3072609 downstream gene variant C/A snv 0.28 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs4648308 0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs4305745 0.882 0.080 6 132572573 downstream gene variant G/A snv 0.55 4
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
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
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs1212171 0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs1187323 0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs25532 0.851 0.160 17 30237152 upstream gene variant G/A snv 6.3E-02 5
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5