Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs16917496 0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 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
rs1206846668 0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs755001634 0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 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
rs200928781 0.752 0.240 22 28695800 missense variant T/A;C;G snv 2.4E-05 11
rs3824662 0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs4846049 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs1043618 0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs3731217 0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs10828317 0.776 0.280 10 22550699 missense variant T/C snv 9
rs1142345 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs2069727 0.763 0.320 12 68154443 intron variant T/A;C snv 9