Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs3745274 0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 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
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
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
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
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