Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
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 27
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 26
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 24
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 23
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 23