Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs10144436 1.000 0.040 14 95090065 3 prime UTR variant C/A snv 2.9E-02 1
rs263232 1.000 0.040 8 130795923 intron variant C/A snv 6.7E-02 1
rs10852889 1.000 0.040 17 6997526 intron variant C/A;G;T snv 1
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs6189 0.827 0.240 5 143400774 missense variant C/A;T snv 4.0E-06; 1.8E-02 6
rs2251177 1.000 0.040 3 114139503 missense variant C/A;T snv 8.0E-06; 0.99 1
rs3100127 1.000 0.040 1 202191842 upstream gene variant C/A;T snv 1
rs6812849 1.000 0.040 4 165951384 intron variant C/A;T snv 1
rs717947 1.000 0.040 4 33652135 intron variant C/A;T snv 1
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2267735 0.925 0.120 7 31095890 intron variant C/G snv 0.47 2
rs4606 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1876831 0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 4
rs7866350 1.000 0.040 9 98221544 intron variant C/G;T snv 0.20 1
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs17070145 0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs5574 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 5