Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs1058205 0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1982151 0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 1
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs3213764 0.925 0.080 12 14434367 missense variant A/G snv 0.47 0.42 1
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs11096957 0.790 0.160 4 38774870 missense variant T/G snv 0.42 0.41 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs11096955 0.851 0.200 4 38774486 missense variant T/C;G snv 4.3E-06; 0.41 1
rs6465657 0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 3
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 1
rs10948059 0.925 0.080 6 42960723 upstream gene variant C/G;T snv 0.39 1
rs2854746 0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 1
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 4
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 1