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
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
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
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 21
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 19
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 19
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 17
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 15
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 15
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 13
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 13
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 13
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 13
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 12