Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908670 0.882 0.080 11 68363784 missense variant G/A snv 3
rs80358313 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 2
rs201320326 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 1
rs121908665 1.000 0.120 11 68403606 missense variant C/T snv 1
rs121908664 1.000 0.120 11 68389949 missense variant G/A snv 1
rs1318906451 1.000 0.120 11 68389900 missense variant T/A snv 4.0E-06 1
rs397514665 1.000 0.120 11 68363791 missense variant C/T snv 1.2E-05 1
rs746701187 1.000 0.120 11 68410019 missense variant T/C snv 4.0E-06 1
rs545508982 1.000 0.120 11 68389980 stop gained G/A;T snv 4.0E-06; 8.0E-06 1
rs1470530779 1.000 0.120 11 68406769 missense variant G/A snv 4.0E-06 1
rs1158745675 1.000 0.120 11 68386367 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs121908671 0.851 0.120 11 68357801 missense variant G/A snv 1
rs121908672 0.925 0.080 11 68357802 missense variant C/T snv 1
rs121908669 1.000 0.040 11 68357672 missense variant G/C snv 1
rs121908673 0.925 0.160 11 68363818 missense variant C/T snv 1
rs1332274863 1.000 0.080 11 68386441 missense variant G/A snv 4.0E-06 1
rs989864153 1.000 0.080 11 68406592 missense variant C/A;T snv 4.0E-06 1
rs121908668 0.882 0.240 11 68357673 missense variant G/T snv 1
rs80358309 1.000 0.080 11 68390032 missense variant G/A snv 4.0E-06 1
rs80358314 1.000 0.080 11 68406572 missense variant T/G snv 1
rs28939709 0.925 0.080 11 68436987 missense variant G/A snv 8.0E-06 1
rs768615287 0.925 0.160 11 68429695 missense variant G/A;T snv 4.0E-06 1
rs80358305 0.882 0.160 11 68348188 missense variant C/T snv 1
rs80358310 1.000 0.080 11 68403502 missense variant C/T snv 1.2E-05 1
rs774342727 1.000 0.080 11 68386564 missense variant G/A;T snv 4.0E-06; 2.0E-05 1