Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 10
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs61750200 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 8
rs768435443 0.807 0.080 1 94055128 missense variant A/G snv 4.0E-06 8
rs201471607 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 7
rs61750130 0.807 0.080 1 94031110 missense variant G/A snv 2.4E-04 2.3E-04 7
rs61750641 0.790 0.080 1 94005499 missense variant C/T snv 3.5E-04 4.7E-04 7
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 7
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 7
rs281865377 0.807 0.080 1 94029447 frameshift variant G/-;GG delins 2.1E-05 6
rs61751383 0.827 0.080 1 94005500 stop gained G/A snv 2.8E-05 1.4E-05 6
rs76157638 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 6
rs1057518767 0.851 0.120 1 94098874 missense variant A/T snv 5
rs1762111 0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 5
rs398123339 0.851 0.120 1 94113068 splice acceptor variant T/C snv 4.0E-06 5
rs560426 0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs61748558 0.827 0.080 1 94063224 missense variant C/T snv 4.0E-06 7.0E-06 5
rs61750654 0.925 0.120 1 94000870 stop gained G/A snv 2.0E-05 7.0E-06 5
rs61751408 0.851 0.080 1 94005509 missense variant G/A snv 2.0E-04 1.7E-04 5
rs1800552 0.851 0.080 1 94010821 missense variant C/T snv 1.6E-03 1.5E-03 4
rs1801269 0.851 0.080 1 94041345 missense variant C/A;T snv 3.1E-04; 4.0E-06 4
rs281865404 0.851 0.080 1 94014675 missense variant GG/CA mnv 4
rs28938473 0.882 0.040 1 94007731 missense variant G/A snv 3.0E-03 3.6E-03 4
rs55732384 0.851 0.080 1 94111561 missense variant G/A snv 1.6E-05 2.1E-05 4