Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs1060505041 0.716 0.400 19 13136099 missense variant C/A;T snv 34
rs1064795104 0.790 0.440 2 72498492 stop gained A/C snv 17
rs1064796765 0.763 0.240 14 102002950 missense variant G/A snv 19
rs1085307135 0.882 0.160 8 143818255 missense variant C/T snv 5
rs1085307138 0.807 0.160 8 143817591 splice donor variant C/T snv 9
rs1085307139 0.925 0.040 8 143817380 frameshift variant -/C delins 5
rs1131691804 0.807 0.200 15 48463123 missense variant G/A snv 6
rs1131692272 0.851 0.240 2 100006808 missense variant C/T snv 8
rs113993993 0.851 0.040 7 66994210 splice donor variant A/C;G snv 4.0E-06; 3.9E-03 9
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
rs1158061584 13 32443086 frameshift variant T/-;TT delins 1
rs119103263 0.827 0.240 1 11992659 missense variant C/T snv 17
rs119473033 0.827 0.320 2 216478216 stop gained G/T snv 8.0E-05 1.3E-04 11
rs120074160 0.925 7 66994286 stop gained T/A snv 1.7E-04 1.0E-03 6
rs121434616 0.925 0.080 X 120544179 stop gained G/A snv 6
rs121908216 0.882 0.200 19 13235702 missense variant C/T snv 7
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121912854 0.851 0.200 3 48592915 stop gained G/A snv 1.2E-05 7.0E-06 16
rs121912855 0.851 0.200 3 48575218 missense variant G/A snv 2.0E-05 7.0E-06 15
rs121913115 1.000 0.120 4 1801928 missense variant A/G snv 2
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 35
rs121913528 0.851 0.160 12 25227349 missense variant C/A;T snv 11
rs121918454 0.742 0.280 12 112450395 missense variant C/A;G;T snv 16
rs121918457 0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 18