Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2679757 0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs430397 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs121918664 0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1346044973 0.851 0.160 5 1294158 missense variant G/A snv 1.1E-05 4
rs675520 0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4646038 0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131