Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24