Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs775097754 1.000 0.160 5 132378362 intron variant T/A snv 4.0E-05 1.4E-05 1
rs1057519051 0.882 0.200 5 132390825 stop gained T/G snv 3
rs1057516765 1.000 0.160 5 132378475 stop gained C/G snv 1
rs1057518297 1.000 0.160 5 132390889 stop gained C/T snv 1
rs121908886 1.000 0.160 5 132387044 stop gained C/T snv 4.0E-05 4.9E-05 1
rs121908887 1.000 0.160 5 132390838 stop gained -/A delins 1
rs121908893 1.000 0.160 5 132385435 stop gained C/A;T snv 5.3E-04; 1.2E-04 1
rs1253026669 1.000 0.160 5 132370224 stop gained C/G;T snv 1
rs1321705165 1.000 0.160 5 132370363 stop gained G/A;T snv 1.7E-05 7.0E-06 1
rs1554085942 1.000 0.160 5 132370157 stop gained G/A snv 1
rs1554086010 1.000 0.160 5 132370333 stop gained C/T snv 1
rs1554088165 1.000 0.160 5 132390809 stop gained G/A snv 1
rs386134212 1.000 0.160 5 132387065 stop gained C/T snv 1.6E-05 1
rs72552722 1.000 0.160 5 132369984 stop gained C/G snv 8.0E-06 1
rs72552727 1.000 0.160 5 132378380 stop gained G/A snv 8.0E-06 1
rs763224132 1.000 0.160 5 132393683 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 1
rs878853249 1.000 0.160 5 132385334 stop gained A/T snv 1
rs114269482 1.000 0.160 5 132385370 missense variant C/T snv 9.1E-05 1.8E-04 1
rs11568520 1.000 0.160 5 132370023 missense variant C/G snv 1.2E-04 4.9E-05 1
rs1178584184 1.000 0.160 5 132378412 missense variant C/T snv 8.0E-06 7.0E-06 1
rs121908888 1.000 0.160 5 132384281 missense variant A/G snv 8.0E-06 7.0E-06 1
rs121908889 1.000 0.160 5 132384155 missense variant G/A snv 4.4E-05 2.8E-05 1
rs121908890 1.000 0.160 5 132384154 missense variant C/T snv 4.0E-06 1
rs121908891 1.000 0.160 5 132390833 missense variant G/A snv 1.6E-05 2.1E-05 1
rs144547521 1.000 0.160 5 132390830 missense variant C/T snv 8.0E-05 6.3E-05 1