Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013210 1.000 0.040 8 24259209 intergenic variant G/A;C;T snv 1
rs10280089 1.000 0.040 7 38667217 intergenic variant C/A;T snv 1
rs10440635 1.000 0.040 5 40490688 intron variant G/A snv 0.56 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 1
rs11249215 1.000 0.040 1 24970693 non coding transcript exon variant G/A snv 0.44 1
rs11742270 1.000 0.040 5 35881341 downstream gene variant G/A snv 0.20 1
rs12141575 1.000 0.040 1 67281753 downstream gene variant G/A snv 0.31 1
rs12574073 0.925 0.120 11 128449583 regulatory region variant C/T snv 0.11 1
rs13001372 1.000 0.040 2 62341086 TF binding site variant A/G snv 0.59 1
rs13093489 1.000 0.040 3 27753416 intergenic variant C/A snv 0.35 1
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 1
rs2242944 1.000 0.040 21 39093252 intergenic variant G/A snv 0.46 1
rs2402752 1.000 0.040 7 124799545 regulatory region variant T/A;C snv 1
rs2531875 1.000 0.040 17 27821141 intron variant G/A;T snv 1
rs2857151 0.925 0.160 6 32795737 intergenic variant A/C;G snv 1
rs378108 1.000 0.040 21 39097594 intergenic variant A/G snv 0.42 1
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 1
rs6502398 1.000 0.040 17 14832175 upstream gene variant A/C;T snv 1
rs657075 0.925 0.120 5 132094425 regulatory region variant G/A snv 8.5E-02 1
rs6759298 1.000 0.040 2 62341310 regulatory region variant G/A;C snv 1
rs769178 1.000 0.040 6 31579737 downstream gene variant G/T snv 8.3E-02 1
rs7743761 1.000 0.040 6 31368323 intron variant C/A snv 0.31 1
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs9901869 0.925 0.120 17 47497840 intergenic variant G/A snv 0.56 1
rs17095830 1.000 0.040 12 45381125 intron variant A/G snv 7.9E-02 1