Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17171329 1.000 0.040 7 38316944 downstream gene variant C/T snv 7.3E-02 1
rs17171331 1.000 0.040 7 38323356 upstream gene variant T/C snv 1
rs17496969 1.000 0.040 7 38324688 upstream gene variant T/C snv 5.5E-02 1
rs1860517 1.000 0.040 7 38291209 downstream gene variant A/G snv 0.53 1
rs2027801 1.000 0.040 7 142712861 upstream gene variant G/A snv 0.48 1
rs2191312 1.000 0.040 7 38327658 intron variant C/T snv 0.26 1
rs2213212 1.000 0.040 7 142698925 downstream gene variant A/C snv 0.63 1
rs2240832 1.000 0.040 7 38289412 downstream gene variant T/C snv 0.27 1
rs2240839 1.000 0.040 7 38302324 upstream gene variant A/G snv 0.45 1
rs2240848 1.000 0.040 7 38321866 upstream gene variant A/G snv 5.5E-02 1
rs2240850 1.000 0.040 7 38324147 upstream gene variant C/A;G;T snv 1
rs2240851 1.000 0.040 7 38324328 upstream gene variant A/G;T snv 1
rs2248839 1.000 0.040 7 38301625 upstream gene variant C/T snv 0.85 1
rs2331599 1.000 0.040 14 22268778 intron variant T/C snv 0.39 1
rs2392545 1.000 0.040 7 38303396 upstream gene variant G/A snv 0.33 1
rs2392546 1.000 0.040 7 38303484 upstream gene variant G/A snv 0.14 1
rs2534567 1.000 0.040 7 38319355 upstream gene variant C/A snv 0.18 1
rs2534568 1.000 0.040 7 38320039 upstream gene variant G/A snv 0.18 1
rs2534575 1.000 0.040 7 38331873 upstream gene variant T/A;C snv 1
rs2534578 1.000 0.040 7 38333930 upstream gene variant T/A;C snv 1
rs2734222 1.000 0.040 7 142780026 upstream gene variant T/A;C snv 1
rs2734224 1.000 0.040 7 142780878 upstream gene variant A/C;G snv 1
rs2735179 1.000 0.040 7 38325004 upstream gene variant T/C snv 0.29 1
rs2736964 1.000 0.040 7 38305168 upstream gene variant T/C snv 0.51 1
rs2736969 1.000 0.040 7 38304355 upstream gene variant A/C snv 0.11 1