Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs577492 1.000 0.120 1 156130948 intron variant T/C snv 0.22 1
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs121909362
GHR
0.827 0.160 5 42699919 missense variant C/T snv 3.9E-03 4.1E-03 5
rs33958176 1.000 0.120 15 98911384 missense variant G/A snv 1.6E-03 1.7E-03 1
rs114025919
GHR
1.000 0.120 5 42688992 missense variant G/T snv 3.0E-04 1.1E-03 1
rs536639583 0.882 0.160 2 176092922 missense variant G/C snv 1.9E-04 6.7E-04 4
rs145730800 1.000 0.120 16 89283963 missense variant G/A snv 5.2E-05 1.4E-04 1
rs201151136 1.000 0.120 8 19458486 missense variant T/C snv 1.4E-04 1.2E-04 1
rs577421663
GHR
1.000 0.120 5 42695051 missense variant G/A snv 2.0E-05 9.8E-05 1
rs104894419 0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs372703574 0.851 0.160 20 38146858 missense variant G/A snv 4.8E-05 6.3E-05 4
rs780108348 1.000 0.120 2 15402229 stop gained G/A snv 1.2E-05 4.2E-05 1
rs121918010 0.827 0.200 1 21573781 missense variant T/C snv 7.2E-05 4.2E-05 5
rs540473875
GHR
1.000 0.120 5 42718502 missense variant A/G snv 4.1E-04 4.2E-05 1
rs122460151 0.851 0.280 X 2958423 missense variant C/G snv 7.1E-05 3.8E-05 5
rs151241066 1.000 0.120 1 220143003 missense variant G/A snv 2.0E-05 3.5E-05 1
rs557914261 0.925 0.160 19 40458393 missense variant G/A snv 2.8E-05 3
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs75028043
GHR
1.000 0.120 5 42688959 missense variant C/T snv 2.1E-04 2.1E-05 1
rs121909173 0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs387906918 0.925 0.120 16 88804027 missense variant G/A snv 7.0E-06 2
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 16
rs137853223 0.851 0.160 17 63917337 missense variant C/T snv 7.0E-06 4
rs755905735 0.851 0.160 17 63917338 missense variant G/A snv 8.0E-06 7.0E-06 4