Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 33
rs543860009 0.742 0.320 2 178589003 stop gained G/A;T snv 33
rs121908188 0.742 0.360 1 25809753 missense variant G/A;C snv 1.8E-04 25
rs199564797 0.742 0.360 1 25809150 missense variant G/A snv 1.2E-05 1.4E-05 25
rs745886248 0.742 0.360 1 25811710 missense variant G/A;C;T snv 4.3E-06; 4.3E-06; 4.3E-06 25
rs781565158 0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 21
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 19
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17
rs1563221666 0.882 0.120 8 22162694 missense variant C/T snv 14
rs59962885
DES
0.807 0.200 2 219420939 missense variant G/A;C;T snv 6.8E-05 8
rs757082154 1.000 0.120 2 178527491 stop gained G/A snv 1.2E-05 8
rs80338962 0.742 0.240 17 63941508 missense variant T/C snv 8
rs386834236
GAA
0.882 0.120 17 80104542 intron variant T/G snv 3.4E-03 3.8E-03 6
rs104894299 0.827 0.120 11 47448079 missense variant G/T snv 1.6E-03 1.5E-03 5
rs55960271 0.882 0.120 7 143351678 stop gained C/A;T snv 4.0E-06; 2.9E-03 5
rs118192177 0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05 4
rs121909092 0.882 0.120 19 10793829 missense variant G/A snv 4
rs121918312 0.776 0.160 10 119672373 missense variant C/A;T snv 4
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 4
rs2754158 0.882 0.080 14 23424876 missense variant G/A;C;T snv 1.2E-05 4
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 4
rs375014127 1.000 0.120 11 22262162 missense variant G/A;T snv 4.0E-06; 6.8E-05 4
rs60682848 0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 4