Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs137854466 0.724 0.320 15 48411280 stop gained G/A;C snv 4.0E-05; 8.0E-06 23
rs112550005 0.742 0.240 15 48425829 stop gained G/A snv 18
rs727503057 0.708 0.280 15 48505106 missense variant G/A snv 7.0E-06 16
rs1566911709 0.742 0.240 15 48495502 frameshift variant T/- delins 15
rs727503054 0.732 0.200 15 48420752 missense variant A/G;T snv 1.6E-05 15
rs113422242 0.763 0.240 15 48510065 stop gained G/A snv 7.0E-06 14
rs1555397413 0.732 0.280 15 48470705 missense variant T/C snv 13
rs137854461 0.790 0.280 15 48437026 missense variant T/C snv 12
rs137854480 0.742 0.200 15 48537629 missense variant G/A snv 11
rs397515804 0.776 0.200 15 48472628 missense variant C/A;T snv 11
rs730880099 0.742 0.200 15 48510125 missense variant G/A snv 11
rs113812345 0.790 0.160 15 48513591 stop gained G/A snv 10
rs1555398397 0.807 0.240 15 48485436 missense variant C/T snv 10
rs193922185 0.752 0.200 15 48505037 missense variant G/A snv 10
rs397515757 0.752 0.200 15 48515382 splice region variant C/T snv 10
rs397515789 0.776 0.240 15 48488112 splice donor variant C/A;T snv 10
rs794728195 0.752 0.200 15 48495155 missense variant G/A snv 10
rs1085308004 0.807 0.240 15 48425420 missense variant A/G snv 9
rs111401431 0.763 0.200 15 48468097 missense variant G/A snv 9
rs111984349 0.763 0.200 15 48415759 missense variant C/T snv 9
rs113543334 0.763 0.200 15 48432944 missense variant A/G snv 9
rs140583 0.763 0.200 15 48495219 stop gained G/A snv 9
rs1555400373 0.763 0.200 15 48515393 missense variant A/G snv 9