Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
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
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9