Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs3129882 0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs707928 0.827 0.320 6 31774813 intron variant A/G snv 0.47 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs13195441 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 2
rs3806624 0.925 0.200 3 27723132 upstream gene variant A/G snv 0.61 2