Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25
rs80338903 0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 17
rs137852832 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 17
rs121918327 0.776 0.240 4 122742955 stop gained C/T snv 2.8E-05 1.4E-05 12
rs768933093 0.807 0.240 12 76348214 missense variant G/A snv 4.8E-05 4.9E-05 10
rs386834158 0.851 0.280 12 88077790 frameshift variant T/- delins 2.2E-05 7.0E-06 10
rs386834061 0.925 0.360 8 99868312 stop gained C/T snv 2.1E-05 10
rs150726175 0.776 0.200 1 9982630 missense variant G/A snv 7.0E-04 8.5E-04 9
rs138504221 0.807 0.280 17 80212128 missense variant A/G snv 9.6E-05 1.5E-04 9
rs1057518939 1.000 0.040 8 99511424 frameshift variant A/- del 9
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 8
rs397515360 0.807 0.160 8 86643781 frameshift variant G/- del 1.8E-03 8
rs886039794 0.851 0.480 8 85109594 splice acceptor variant G/C snv 8
rs2723341 0.807 0.160 15 71811481 splice acceptor variant A/C snv 5.3E-04 5.1E-04 8
rs752914124 0.827 0.280 17 80210679 stop gained GGAGGTCCTTG/- del 8
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 7
rs62645748 0.807 0.080 1 197434706 missense variant G/A snv 2.1E-04 2.2E-04 7
rs61751383 0.827 0.080 1 94005500 stop gained G/A snv 2.8E-05 1.4E-05 6
rs76157638 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 6
rs764109067 0.851 0.280 3 94036664 missense variant G/A;T snv 4.0E-06 6