Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs776746 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs2853677 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs10759932 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15