Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12035317 1.000 0.120 1 113553475 intron variant T/G snv 0.22 1
rs12063329 1.000 0.120 1 150030478 intergenic variant T/C snv 0.13 1
rs12131057 1.000 0.120 1 38158457 intron variant G/A snv 0.20 1
rs12140275 1.000 0.120 1 38168207 intergenic variant A/T snv 0.21 1
rs1217407 1.000 0.120 1 113851126 intron variant A/G snv 0.77 1
rs1217413 1.000 0.120 1 113815128 intron variant G/A snv 0.82 1
rs1217418 0.925 0.120 1 113858609 intron variant A/G snv 0.53 0.57 1
rs1230647 1.000 0.120 1 113711017 intron variant C/T snv 0.78 1
rs12565755 1.000 0.120 1 60576203 intron variant T/C;G snv 1
rs12566340 0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 1
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2105325 1.000 0.120 1 173380586 intergenic variant A/C;G snv 1
rs2240335 1.000 0.120 1 17348042 synonymous variant C/A snv 0.39 0.37 1
rs2240336 1.000 0.120 1 17347907 intron variant C/T snv 0.43 0.45 1
rs2240339 1.000 0.120 1 17347613 intron variant C/T snv 0.36 1
rs227163 1.000 0.120 1 7901146 intergenic variant C/G;T snv 1
rs2301888 1.000 0.120 1 17346235 intron variant G/A snv 0.31 1
rs2317230 1.000 0.120 1 157705207 upstream gene variant G/T snv 0.56 1
rs2797409 1.000 0.120 1 113787580 intron variant T/C snv 0.27 1
rs28411352 1.000 0.120 1 37812907 3 prime UTR variant C/T snv 0.23 1
rs2843401 1.000 0.120 1 2596694 splice region variant T/C snv 0.61 0.59 1
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 1
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 1