Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894845 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs104894828 0.882 0.160 X 101398467 missense variant C/A;T snv 3
rs199473684 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 3
rs28935485 0.925 0.160 X 101398534 missense variant G/C snv 3
rs28935490 1.000 0.160 X 101398432 missense variant C/A;T snv 3.0E-03; 5.4E-06 3
rs398123226 0.882 0.160 X 101398403 missense variant G/C;T snv 3
rs104894830 0.925 0.160 X 101398483 missense variant T/C snv 2
rs104894846 0.925 0.160 X 101398481 missense variant C/T snv 2
rs104894847 0.925 0.160 X 101407846 missense variant C/G snv 2
rs397515870 1.000 0.160 X 101400692 missense variant G/C;T snv 2
rs727504348 0.925 0.160 X 101397982 missense variant C/T snv 2
rs104894827 1.000 0.160 X 101398033 missense variant G/A snv 1
rs104894829 1.000 0.160 X 101407773 stop gained C/T snv 1
rs104894831 1.000 0.160 X 101407786 missense variant G/A snv 1
rs104894832 1.000 0.160 X 101398387 missense variant C/G;T snv 1
rs104894834 1.000 0.160 X 101403846 missense variant G/A snv 1
rs104894835 1.000 0.160 X 101407803 missense variant T/C snv 1
rs104894836 1.000 0.160 X 101407738 missense variant A/C snv 1
rs104894837 1.000 0.160 X 101401743 missense variant G/A snv 1
rs104894838 1.000 0.160 X 101400699 missense variant A/C snv 1
rs104894839 1.000 0.160 X 101398508 stop gained C/A;T snv 1
rs104894840 1.000 0.160 X 101398906 missense variant C/G;T snv 1
rs104894841 1.000 0.160 X 101398907 stop gained G/A snv 9.5E-06 1
rs104894842 1.000 0.160 X 101398079 stop gained C/T snv 1
rs104894843 1.000 0.160 X 101398075 stop gained G/A;C snv 1