Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 26
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 22
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 19
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 12
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 11
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 8
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 7
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 6
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 6
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 6
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 6
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 5
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 5
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 4
rs17700633 0.882 0.120 18 60262199 intergenic variant G/A snv 0.28 4
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 4
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 4