Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs2162440 1.000 0.160 18 37634043 intron variant A/G;T snv 1
rs6430612 1.000 0.160 2 136248628 intergenic variant C/T snv 0.44 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs10818488 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs2900180 0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs727088 0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 8
rs34794968 0.925 0.200 18 69863790 3 prime UTR variant C/A snv 0.36 2
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs762623 1.000 0.160 6 36677689 non coding transcript exon variant G/A snv 0.12 2
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101