Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2276466 0.732 0.320 16 13949318 3 prime UTR variant C/A;G snv 15
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188