Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34516117 1.000 0.120 11 2847771 missense variant C/T snv 1.6E-04 6.1E-04 1
rs143709408 0.882 0.200 11 2527999 missense variant C/T snv 1.6E-04 3.6E-04 5
rs199473443 1.000 0.120 11 2445117 missense variant C/T snv 1.7E-04 1
rs140452381 1.000 0.120 11 2588815 missense variant C/T snv 8.0E-05 1.5E-04 1
rs199472728 0.925 0.120 11 2572885 missense variant A/G snv 1.8E-04 1.3E-04 2
rs199472706 0.925 0.120 11 2571391 missense variant C/T snv 4.0E-06 1.0E-04 3
rs199473671 1.000 0.120 11 2445234 missense variant G/A snv 6.0E-05 6.5E-05 1
rs199472735 1.000 0.120 11 2572925 missense variant C/A snv 5.2E-05 6.3E-05 1
rs120074190 0.882 0.120 11 2778009 missense variant G/A snv 4.8E-05 5.6E-05 3
rs199472736 1.000 0.120 11 2572940 missense variant G/A snv 4.4E-05 5.6E-05 1
rs199473484 1.000 0.120 11 2847875 missense variant G/A snv 1.6E-05 4.9E-05 1
rs199473464 1.000 0.120 11 2572933 missense variant G/A snv 1.6E-05 4.9E-05 1
rs151344631 0.827 0.200 11 2571333 missense variant G/A snv 8.0E-06 3.5E-05 3
rs199473482 1.000 0.120 11 2777991 missense variant G/A snv 1.6E-05 3.5E-05 1
rs150172393 0.925 0.120 11 2570733 missense variant C/T snv 2.8E-05 3.5E-05 1
rs199472692 1.000 0.120 11 2570634 missense variant G/A snv 1.6E-05 2.8E-05 1
rs199472813 1.000 0.120 11 2778011 missense variant G/A;C snv 8.0E-06 2.1E-05 1
rs199472796 1.000 0.120 11 2775990 missense variant G/A snv 2.7E-05 2.1E-05 1
rs199472737 1.000 0.120 11 2572942 missense variant C/T snv 3.6E-05 2.1E-05 1
rs120074187 0.882 0.120 11 2572963 missense variant G/A snv 4.8E-05 2.1E-05 2
rs199472821 1.000 0.120 11 2847848 missense variant G/A snv 1.1E-05 1.4E-05 1
rs397508097 0.807 0.120 11 2768917 stop gained C/T snv 2.8E-05 1.4E-05 6
rs199472696 0.851 0.120 11 2570670 missense variant C/T snv 4.0E-06 1.4E-05 3
rs199473449 1.000 0.120 11 2527938 missense variant G/A snv 4.0E-06 1.4E-05 1
rs397508118 0.851 0.120 11 2570720 frameshift variant GCGCT/- delins 1.4E-05 4