Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555545033 0.807 0.160 17 40088306 missense variant C/T snv 7
rs121909362
GHR
0.827 0.160 5 42699919 missense variant C/T snv 3.9E-03 4.1E-03 5
rs121912889 0.851 0.160 12 47974234 missense variant T/C snv 4
rs121917883 0.851 0.160 3 172447803 missense variant G/A;T snv 2.8E-05 4
rs137853223 0.851 0.160 17 63917337 missense variant C/T snv 7.0E-06 4
rs372703574 0.851 0.160 20 38146858 missense variant G/A snv 4.8E-05 6.3E-05 4
rs536639583 0.882 0.160 2 176092922 missense variant G/C snv 1.9E-04 6.7E-04 4
rs755905735 0.851 0.160 17 63917338 missense variant G/A snv 8.0E-06 7.0E-06 4
rs1218653273 0.925 0.160 17 42292005 missense variant C/T snv 4.0E-06 3
rs121917843 0.882 0.160 5 177994231 missense variant G/A snv 4.0E-06 3
rs557914261 0.925 0.160 19 40458393 missense variant G/A snv 2.8E-05 3
rs587777614 0.882 0.160 10 68416703 frameshift variant G/- delins 3
rs587779348 0.882 0.160 2 46623765 frameshift variant T/- delins 3
rs587779356 0.882 0.160 2 46619676 frameshift variant -/GG delins 3
rs759838407 0.925 0.160 13 108209756 frameshift variant AG/-;AGAG delins 3
rs137853221 0.925 0.160 17 63917803 missense variant T/C snv 2
rs137853222 0.925 0.160 17 63918072 missense variant C/A;G snv 2
rs180177456 0.925 0.160 1 247424426 missense variant G/A snv 2
rs886037910
GHR
0.925 0.160 5 42699943 missense variant T/C snv 2
rs1131691804 0.807 0.200 15 48463123 missense variant G/A snv 8
rs2076738
TG
0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 6
rs587779351 0.851 0.200 5 83105046 missense variant T/C snv 1.6E-05 6
rs121918010 0.827 0.200 1 21573781 missense variant T/C snv 7.2E-05 4.2E-05 5
rs2076739
TG
0.827 0.200 8 132971804 missense variant T/A snv 5
rs397514461 0.827 0.200 Y 640842 missense variant G/C snv 5