Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59962885
DES
0.807 0.200 2 219420939 missense variant G/A;C;T snv 6.8E-05 11
rs61672878 0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs80338957 0.776 0.160 17 63957427 missense variant G/A snv 11
rs104894369 0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs113994099 0.827 0.240 15 89320883 missense variant T/C snv 10
rs28937581 0.827 0.160 2 71570300 missense variant G/T snv 1.2E-05 9
rs914586984 1.000 0.120 17 63959275 missense variant G/C;T snv 9
rs121434589 0.851 0.200 17 10535137 missense variant C/T snv 8
rs142000963 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs137853305 0.851 0.120 9 35685529 missense variant G/A snv 7
rs118192170 0.882 0.120 19 38584989 missense variant T/A;C snv 6
rs121913003
DES
0.882 0.200 2 219421532 missense variant C/T snv 6
rs137853306 0.882 0.080 9 35689265 missense variant C/T snv 6
rs397514677 0.851 0.400 11 4023928 missense variant A/G snv 6
rs57965306
DES
0.925 0.160 2 219421365 missense variant G/A;C snv 2.8E-05 6
rs57983345 0.851 0.160 1 156115034 missense variant A/G snv 6
rs121908211 0.882 0.080 19 13371744 missense variant C/T snv 5
rs138977195 1.000 0.120 16 56887967 missense variant G/A snv 3.7E-04 4.1E-04 5
rs1057518957 1.000 0.040 2 232535143 missense variant G/T snv 4
rs1373863123 1.000 0.080 7 5529540 missense variant G/A snv 4
rs199474714 0.925 0.080 1 154173113 missense variant C/T snv 4
rs746438011 0.882 0.120 6 152430672 missense variant A/G;T snv 1.2E-05 4
rs75586164 0.925 0.080 5 70070651 missense variant C/T snv 1.3E-04 4
rs760361706 22 46235326 missense variant G/C snv 4.0E-06 4
rs117184249 1.000 0.120 6 152401278 missense variant C/T snv 9.3E-04 4.0E-04 3