Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs2231137 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs806321 0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs41289586 0.882 0.160 3 43577066 missense variant C/T snv 1.8E-02 1.9E-02 3
rs13255292 0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs2070770 0.925 0.120 11 60463058 synonymous variant C/T snv 7.1E-02 5.4E-02 2
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1883112 0.851 0.200 22 36860804 intron variant G/A snv 0.39 4
rs1323292 0.882 0.160 1 192571891 intron variant G/A snv 0.86 3
rs143002189 1.000 0.120 6 137881310 missense variant G/A snv 4.3E-04 4.4E-04 3
rs1390458638 0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 2
rs1880030 0.925 0.120 12 122046634 intron variant G/A snv 0.39 2
rs2681416 0.925 0.120 3 122098766 intron variant G/A snv 0.26 2
rs3025684 1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 2
rs777500092 1.000 0.120 2 25246231 missense variant G/A snv 8.0E-06 2
rs2228479 0.763 0.280 16 89919532 missense variant G/A;C snv 7.8E-02; 4.0E-06 11