Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2517485 1.000 0.120 6 31106324 downstream gene variant C/A;T snv 1
rs2523864 1.000 0.120 6 31050769 upstream gene variant C/T snv 0.47 1
rs2611215 1.000 0.120 4 165653115 intron variant A/G snv 0.83 1
rs2844697 1.000 0.120 6 30964532 upstream gene variant C/T snv 0.44 1
rs2858308 1.000 0.120 6 32702223 downstream gene variant G/T snv 0.10 1
rs286405 1.000 0.120 5 35577155 intergenic variant C/T snv 0.54 1
rs3094122 1.000 0.120 6 30760583 intron variant T/G snv 0.21 1
rs3094621 1.000 0.120 6 30360976 upstream gene variant T/C snv 8.4E-02 1
rs3095329 1.000 0.120 6 30726039 upstream gene variant A/G snv 0.27 1
rs3104402 1.000 0.120 6 32713899 upstream gene variant T/G snv 0.96 1
rs3115673 1.000 0.120 6 31842308 downstream gene variant G/T snv 0.23 1
rs3130837 1.000 0.120 6 28980315 downstream gene variant G/T snv 5.2E-02 1
rs3131063 1.000 0.120 6 30795979 downstream gene variant G/A;C snv 1
rs3132131 1.000 0.120 6 32931708 downstream gene variant A/G snv 0.73 1
rs3132630 1.000 0.120 6 30377341 intergenic variant C/T snv 0.11 1
rs35285258 1.000 0.120 10 6076807 upstream gene variant C/T snv 0.18 1
rs439121 1.000 0.120 6 33225090 intergenic variant A/C snv 0.27 1
rs5790666 1.000 0.120 11 27778324 intron variant G/- delins 0.14 1
rs6547853 1.000 0.120 2 28423934 upstream gene variant G/A snv 0.35 1
rs672797 1.000 0.120 1 81094869 downstream gene variant C/A;T snv 0.63 1
rs6901084 1.000 0.120 6 32769159 intergenic variant C/T snv 0.50 1
rs6903496 1.000 0.120 6 31384997 upstream gene variant G/A snv 5.3E-02 1
rs72853903 1.000 0.120 11 2177435 downstream gene variant C/T snv 0.22 1
rs7356880 1.000 0.120 6 32433550 regulatory region variant C/T snv 7.3E-02 1
rs75352297 1.000 0.120 3 46303660 regulatory region variant T/C snv 9.7E-02 1