Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1799941 0.763 0.280 17 7630105 5 prime UTR variant G/A snv 0.18 11
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1549758 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2774279 0.925 0.080 1 161047766 synonymous variant C/T snv 0.27 0.27 3
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41