Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1116357 1.000 0.080 2 57060276 intergenic variant A/G snv 0.51 1
rs111886096 1.000 0.080 16 53564398 intergenic variant A/G snv 0.13 1
rs11202614 1.000 0.080 10 87995886 upstream gene variant C/T snv 0.14 1
rs11228303 1.000 0.080 11 68632701 regulatory region variant C/G;T snv 9.8E-02 1
rs11240074 1.000 0.080 1 147524657 intergenic variant A/C;G snv 1
rs11265455 1.000 0.080 1 160650361 upstream gene variant A/G snv 0.15 1
rs113932007 1.000 0.080 11 115620719 intergenic variant TT/-;T;TTT;TTTT;TTTTT delins 1
rs1152003 1.000 0.080 3 12435556 downstream gene variant G/C snv 0.56 1
rs11590362 1.000 0.080 1 42742890 upstream gene variant A/G snv 5.9E-02 1
rs116116673 1.000 0.080 5 143951835 intergenic variant T/C snv 1.4E-02 1
rs11619726 1.000 0.080 13 36601856 intergenic variant T/G snv 1.2E-02 1
rs116517707 1.000 0.080 12 116481563 upstream gene variant C/G;T snv 1
rs11820019 1.000 0.080 11 69633990 intergenic variant T/C snv 4.7E-02 1
rs11925227 1.000 0.080 3 171048829 intron variant G/A snv 0.18 1
rs11927173 1.000 0.080 3 23183703 TF binding site variant T/C snv 0.13 1
rs12088739 1.000 0.080 1 51041214 intergenic variant A/G snv 0.13 1
rs12219514 1.000 0.080 10 92706682 downstream gene variant A/G snv 0.45 1
rs12233372 1.000 0.080 3 35853837 intergenic variant T/C snv 8.5E-04 1
rs1225537 1.000 0.080 17 34385098 intergenic variant T/A;C snv 1
rs12277475 1.000 0.080 11 2185703 intergenic variant C/T snv 4.1E-02 1
rs12325830 1.000 0.080 17 56632283 intergenic variant C/T snv 0.46 1
rs1255372 1.000 0.080 10 42496332 downstream gene variant T/C snv 0.71 1
rs12613372 1.000 0.080 2 30845153 intergenic variant C/A;G snv 1
rs12625067 1.000 0.080 20 44315384 upstream gene variant C/A;T snv 1
rs12649012 1.000 0.080 4 70882528 intergenic variant G/A snv 0.85 1