Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386834236
GAA
0.882 0.120 17 80104542 intron variant T/G snv 3.4E-03 3.8E-03 6
rs55960271 0.882 0.120 7 143351678 stop gained C/A;T snv 4.0E-06; 2.9E-03 5
rs121908627
CLTA ; GNE
0.925 0.160 9 36217448 missense variant C/A;T snv 8.9E-04; 1.7E-03 3
rs104894299 0.827 0.120 11 47448079 missense variant G/T snv 1.6E-03 1.5E-03 5
rs149278319 1.000 7 157367416 missense variant C/A;G;T snv 4.0E-06; 1.4E-03 1
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 33
rs150516929 0.807 0.240 11 111908832 missense variant C/T snv 9.1E-04 8.7E-04 1
rs535661345 0.925 0.120 2 237372173 missense variant C/T snv 2.0E-04 2.1E-05 3
rs121908188 0.742 0.360 1 25809753 missense variant G/A;C snv 1.8E-04 25
rs370634440 19 38463499 missense variant G/A;T snv 1.7E-04; 8.0E-06 1
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 4
rs59962885
DES
0.807 0.200 2 219420939 missense variant G/A;C;T snv 6.8E-05 8
rs375014127 1.000 0.120 11 22262162 missense variant G/A;T snv 4.0E-06; 6.8E-05 4
rs139552940 21 46131981 missense variant G/A snv 5.9E-05 4.2E-05 1
rs781565158 0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 21
rs564856283 12 101642495 missense variant G/A;C snv 3.2E-05 3
rs746721983 2 178706629 stop gained G/A snv 2.8E-05 2.1E-05 1
rs121908192 0.925 0.280 16 1985991 missense variant G/A snv 2.8E-05 3.5E-05 1
rs751995154 1.000 0.200 17 7224011 missense variant G/A;C snv 2.8E-05 3.5E-05 3
rs57965306
DES
0.925 0.160 2 219421365 missense variant G/A;C snv 2.8E-05 2
rs545623839 1.000 0.160 17 10533349 stop gained G/A snv 2.4E-05 2
rs104894294 1.000 11 47447853 missense variant G/A snv 2.0E-05 2.1E-05 2
rs118192177 0.851 0.160 19 38496283 missense variant C/G;T snv 2.0E-05 4
rs774521989 21 46132125 missense variant C/T snv 1.6E-05 4.9E-05 1
rs757082154 1.000 0.120 2 178527491 stop gained G/A snv 1.2E-05 8