Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs3733890 0.708 0.480 5 79126136 missense variant G/A snv 0.30 0.28 16
rs1206846668 0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs2231137 0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs1801265 0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs368939818 0.763 0.280 11 49156734 missense variant G/A snv 4.0E-05 2.1E-05 13
rs755001634 0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs861530 0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs2239633 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573 0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs201765376
MTR
0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05 12