Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 8
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 7
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
rs61750654 0.925 0.120 1 94000870 stop gained G/A snv 2.0E-05 7.0E-06 5
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 5
rs201471607 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 4
rs61749409 0.882 0.080 1 94062710 missense variant G/A snv 4.4E-05 2.1E-05 4
rs61751389 0.925 0.040 1 94007722 frameshift variant C/- del 2.8E-05 7.0E-06 4
rs61751406 0.925 0.120 1 94014622 missense variant G/T snv 2.0E-05 2.8E-05 4
rs1762111 0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 3
rs61750138 1.000 1 94030991 splice region variant C/A;T snv 1.2E-05 3
rs61750645 0.925 0.080 1 94001911 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3
rs61751402 0.882 0.080 1 94029515 missense variant C/T snv 6.3E-05 5.6E-05 3
rs61751404 0.882 0.080 1 94021340 missense variant G/A;C snv 3.2E-05; 4.0E-06 3
rs764759172 0.925 0.040 1 94080692 frameshift variant G/- del 3
rs778234759 0.925 0.040 1 94018445 intron variant C/T snv 1.3E-04 3
rs1553186896 1.000 1 94005490 missense variant A/C;G snv 2
rs1553192726 1.000 0.080 1 94063315 stop gained G/T snv 2
rs1553193813 1.000 0.080 1 94077747 stop gained C/T snv 2
rs61748552 1.000 1 94078611 missense variant G/C snv 8.0E-06 8.3E-06 2
rs61749451 0.925 0.080 1 94046922 missense variant G/A;T snv 2.0E-05; 3.6E-05 2
rs61750135 1.000 1 94031027 missense variant A/G snv 1.6E-05 1.4E-05 2
rs1064793014 1 94007707 missense variant T/C snv 1