Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs181681840 1.000 0.160 15 48494269 intron variant G/A;T snv 7.7E-04; 2.0E-05 3.2E-03 1
rs137854475 0.882 0.200 15 48487155 missense variant C/T snv 1.3E-03 1.6E-03 3
rs145942328 1.000 0.160 15 48613072 missense variant C/T snv 5.6E-05 1.2E-04 1
rs564713154 0.925 0.160 15 48489920 stop gained C/A;T snv 1.2E-05 5.6E-05 2
rs201778577 1.000 0.160 15 48495574 stop gained C/A;T snv 3.2E-05 5.6E-05 1
rs149062442 0.925 0.160 15 48415588 stop gained C/A;T snv 2.0E-05 5.6E-05 2
rs193922179 1.000 0.160 15 48510124 missense variant C/T snv 1.4E-05 1
rs112375043 0.925 0.160 15 48472594 stop gained G/A;C;T snv 3.6E-05 1.4E-05 2
rs534811966 1.000 0.160 15 48428350 stop gained G/A;T snv 1.4E-05 1
rs794728204 0.925 0.160 15 48487312 missense variant C/T snv 1.4E-05 2
rs146348130 1.000 0.160 15 48534170 stop gained G/A;T snv 4.0E-06 7.0E-06 1
rs113422242 0.763 0.240 15 48510065 stop gained G/A snv 7.0E-06 14
rs587782946 1.000 0.160 15 48470688 missense variant G/A snv 8.0E-06 7.0E-06 1
rs193922204 0.763 0.200 15 48468542 splice region variant C/T snv 4.0E-06 7.0E-06 9
rs140592 0.925 0.160 15 48489947 missense variant A/G snv 7.0E-06 2
rs397514558 0.851 0.200 15 48490013 missense variant G/A snv 7.0E-06 4
rs1206813753 0.925 0.160 15 48489956 missense variant A/G snv 7.0E-06 2
rs1052480459 0.925 0.160 15 48437837 stop gained C/A;G snv 7.0E-06 2
rs727503057 0.708 0.280 15 48505106 missense variant G/A snv 7.0E-06 16
rs193922228 0.763 0.200 15 48430736 missense variant A/G snv 7.0E-06 9
rs137854464 0.851 0.200 15 48425483 missense variant C/T snv 7.0E-06 5
rs794728280 0.925 0.160 15 48415671 missense variant T/C snv 7.0E-06 2
rs363804 1.000 0.160 15 48441771 missense variant C/T snv 7.0E-06 1
rs1232880706 0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34