Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 48
rs104894419 0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs1057517917 0.925 0.200 12 112450368 missense variant AT/GC mnv 2
rs111033552 0.925 0.120 6 116120105 missense variant A/G snv 2
rs1131691804 0.807 0.200 15 48463123 missense variant G/A snv 8
rs114025919
GHR
1.000 0.120 5 42688992 missense variant G/T snv 3.0E-04 1.1E-03 1
rs1179060441
GHR
1.000 0.120 5 42694934 missense variant C/T snv 8.1E-06 1
rs1211533350 0.827 0.120 4 1805638 synonymous variant C/A snv 4.0E-06 7.0E-06 5
rs1218653273 0.925 0.160 17 42292005 missense variant C/T snv 4.0E-06 3
rs121909173 0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
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
rs121913479 0.763 0.280 4 1804362 missense variant G/A;T snv 4.0E-06 10
rs121913485 0.716 0.400 4 1804372 missense variant A/G snv 18
rs121917843 0.882 0.160 5 177994231 missense variant G/A snv 4.0E-06 3
rs121917883 0.851 0.160 3 172447803 missense variant G/A;T snv 2.8E-05 4
rs121918010 0.827 0.200 1 21573781 missense variant T/C snv 7.2E-05 4.2E-05 5
rs121918456 0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs122460151 0.851 0.280 X 2958423 missense variant C/G snv 7.1E-05 3.8E-05 5
rs1314542724 0.925 0.120 9 35805595 missense variant C/T snv 2
rs137853092 0.851 0.240 17 42787494 missense variant C/G snv 5
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