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
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
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
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
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 7
rs61751383 0.827 0.080 1 94005500 stop gained G/A snv 2.8E-05 1.4E-05 6
rs1762111 0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 5
rs61748558 0.827 0.080 1 94063224 missense variant C/T snv 4.0E-06 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
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
rs61749420 0.851 0.080 1 94060740 missense variant G/A snv 1.6E-05 7.0E-06 4
rs61750146 0.851 0.080 1 94029522 missense variant A/G snv 8.2E-06 7.0E-06 4
rs61751389 0.925 0.040 1 94007722 frameshift variant C/- del 2.8E-05 7.0E-06 4
rs61753038 0.851 0.080 1 94005470 stop gained G/A snv 1.2E-05 7.0E-06 4
rs886044758 0.851 0.080 1 94005511 missense variant A/G snv 4.0E-06 4
rs61750639 0.882 0.080 1 94007710 missense variant C/T snv 8.0E-06 1.4E-05 3
rs1800548 0.925 0.040 1 94077833 missense variant C/T snv 8.3E-04 8.9E-04 2
rs1800549 0.925 0.040 1 94030497 missense variant G/A snv 4.6E-03 1.6E-03 2
rs61750202 0.925 0.040 1 94055245 missense variant C/G;T snv 2.1E-04 2