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
rs1056123575 0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs16940 0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs1213469537 0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs1172398253 0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs3731499 0.925 0.080 3 48184680 missense variant G/A snv 5.7E-05 1.2E-04 3
rs1219211410 0.925 0.080 20 3800494 missense variant T/C snv 3
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs200863613 0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16