Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21