Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1226085679 0.882 0.120 19 45351663 missense variant A/T snv 3
rs8111742 0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs4353229 0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs17728461 0.776 0.120 22 30202563 intron variant C/G snv 0.25 9
rs667282 0.790 0.120 15 78571130 intron variant T/C snv 0.28 9
rs753955 0.776 0.120 13 23719720 regulatory region variant A/G snv 0.50 9
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 10
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs6682925 0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs13042395 0.752 0.160 20 773867 intron variant C/T snv 5.9E-02 13
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 20
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2298881 0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2839698 0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 28