Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs33958176 1.000 0.120 15 98911384 missense variant G/A snv 1.6E-03 1.7E-03 1
rs145730800 1.000 0.120 16 89283963 missense variant G/A snv 5.2E-05 1.4E-04 1
rs387906918 0.925 0.120 16 88804027 missense variant G/A snv 7.0E-06 2
rs587779351 0.851 0.200 5 83105046 missense variant T/C snv 1.6E-05 6
rs587781858 0.742 0.360 17 7669671 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 12
rs587777614 0.882 0.160 10 68416703 frameshift variant G/- delins 3
rs397515453 0.752 0.440 5 68296301 missense variant C/T snv 11
rs397514461 0.827 0.200 Y 640842 missense variant G/C snv 5
rs761695685
GH1
0.925 0.200 17 63918865 intron variant T/C snv 2
rs137853222 0.925 0.160 17 63918072 missense variant C/A;G snv 2
rs137853220 0.882 0.200 17 63917909 missense variant G/A snv 4.0E-06 4
rs137853221 0.925 0.160 17 63917803 missense variant T/C snv 2
rs755905735 0.851 0.160 17 63917338 missense variant G/A snv 8.0E-06 7.0E-06 4
rs137853223 0.851 0.160 17 63917337 missense variant C/T snv 7.0E-06 4
rs121909173 0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs397514487 0.882 0.200 3 52149850 stop gained G/A snv 7.0E-06 3
rs141842220 1.000 0.120 20 5119600 missense variant C/T snv 1
rs754740382 1.000 0.120 6 49459175 missense variant T/C;G snv 8.0E-06; 4.0E-06 1
rs1131691804 0.807 0.200 15 48463123 missense variant G/A snv 8
rs1566902569 0.882 0.160 15 48460299 missense variant C/A snv 9
rs387906623 0.882 0.120 15 48460258 missense variant C/T snv 4
rs121912889 0.851 0.160 12 47974234 missense variant T/C snv 4
rs587779348 0.882 0.160 2 46623765 frameshift variant T/- delins 3
rs587779356 0.882 0.160 2 46619676 frameshift variant -/GG delins 3