Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805014 0.851 0.080 16 27363708 missense variant T/C snv 7.4E-03 1.4E-02 4
rs6871536 0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs324015 0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs2664538 0.827 0.200 20 46011586 missense variant A/G snv 6
rs4065275 0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs12603332 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs4794067 0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs569108 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs4523 0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1207011218 0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43