Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17294280 0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 4
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 3
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 3