Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17700633 0.882 0.120 18 60262199 intergenic variant G/A snv 0.28 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs181914932 1.000 0.040 20 45932640 non coding transcript exon variant T/C snv 1.6E-02 2
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs1974990 1.000 0.040 2 169790406 non coding transcript exon variant G/T snv 0.90 3
rs200950799 1.000 0.040 12 17004185 intergenic variant C/T snv 1.1E-02 3
rs2105903 1.000 0.040 6 32427879 intergenic variant A/T snv 0.14 3
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 5
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs2863389 1.000 0.040 3 166431104 intergenic variant C/T snv 0.17 2
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs3132374 1.000 0.040 6 28900717 downstream gene variant C/G snv 5.3E-02 3
rs4258701 1.000 0.040 18 27895834 intergenic variant C/T snv 0.28 2
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 7
rs4900384 0.882 0.160 14 98032614 intergenic variant A/G snv 0.40 4
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9