Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs120074177 0.925 0.120 11 2570682 missense variant G/A;C snv 4.0E-06 2
rs120074178 0.925 0.120 11 2570719 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 1.6E-05 2
rs120074179 0.925 0.120 11 2572089 missense variant G/A;C;T snv 3
rs120074181 0.925 0.120 11 2572981 missense variant G/A;C snv 2
rs120074184 0.925 0.120 11 2583453 missense variant G/A;C;T snv 2
rs120074185 0.925 0.120 11 2776032 missense variant C/A;T snv 1.1E-05; 1.1E-05 3
rs120074186 0.851 0.120 11 2572979 stop gained G/A;C;T snv 1.6E-05; 4.0E-06; 4.0E-06 4
rs120074187 0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 3
rs120074189 0.851 0.120 11 2778003 missense variant C/T snv 4
rs120074190 0.882 0.120 11 2778009 missense variant G/A snv 4.8E-05 5.6E-05 3
rs120074191 0.925 0.120 11 2445448 missense variant C/T snv 2
rs120074193 0.807 0.120 11 2572870 missense variant G/A;C snv 4.0E-06 7
rs120074194 0.925 0.120 11 2572871 missense variant G/A;T snv 2
rs12720458 0.716 0.240 11 2585264 missense variant A/G snv 4.0E-05 1.4E-05 20
rs12720459 0.807 0.160 11 2583535 missense variant C/A;G;T snv 7
rs1380382303 0.925 0.120 7 150950989 synonymous variant G/A snv 7.0E-06 2
rs139042529 0.925 0.120 11 2570663 stop gained C/A;G;T snv 8.0E-06; 9.4E-04 2
rs147445322 0.882 0.120 11 2847803 missense variant G/A;T snv 7.2E-05; 5.5E-06 4
rs150172393 0.925 0.120 11 2570733 missense variant C/T snv 2.8E-05 3.5E-05 2
rs151344631 0.827 0.200 11 2571333 missense variant G/A snv 8.0E-06 3.5E-05 5
rs17215500 0.807 0.240 11 2768881 stop gained C/G;T snv 1.0E-04 7
rs179489 0.925 0.120 11 2570652 missense variant G/A;C snv 1.2E-05; 4.0E-06 2
rs1800171 0.882 0.120 11 2583545 splice region variant G/A;C;T snv 4.0E-06 3
rs1805127 0.732 0.240 21 34449523 missense variant T/C snv 0.64 2.0E-04 17
rs193922365 0.925 0.120 11 2572970 missense variant C/A;T snv 4.0E-06 2