Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs41293497 0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs80358920 0.732 0.400 13 32346841 stop gained C/G;T snv 12
rs80359200 0.752 0.320 13 32394726 stop gained C/A;G snv 8.0E-06 12
rs28897756 0.752 0.440 13 32379913 splice region variant G/A;C;T snv 4.0E-06 11
rs80358435 0.752 0.440 13 32319154 stop gained G/C;T snv 4.0E-06; 4.0E-06 11
rs80358721 0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 11
rs80358814 0.742 0.440 13 32340212 stop gained G/T snv 8.0E-06 11
rs80358972 0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 11
rs80359212 0.763 0.320 13 32394814 stop gained C/T snv 1.2E-05 4.2E-05 11
rs137853011 0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 10
rs397507404 0.763 0.320 13 32370955 splice acceptor variant G/A;T snv 10
rs41293511 0.763 0.320 13 32363369 missense variant G/A;C snv 7.0E-06 10
rs80358391 0.763 0.320 13 32319109 stop gained G/A;T snv 4.0E-06 10
rs80358427 0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10
rs80358557 0.763 0.320 13 32337464 stop gained C/A;T snv 4.0E-06; 4.0E-06 10
rs80358893 0.763 0.320 13 32341011 stop gained C/G snv 10
rs80359014 0.763 0.320 13 32362596 missense variant A/G;T snv 10
rs80359031 0.763 0.320 13 32363190 missense variant A/T snv 10
rs397507327 0.776 0.280 13 32338598 stop gained G/A;T snv 4.1E-06 9
rs397508045 0.763 0.320 13 32319101 stop gained G/A;T snv 4.0E-06; 4.0E-06 9
rs80358807 0.763 0.280 13 32340146 stop gained C/T snv 9
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 8
rs180177132 0.790 0.280 16 23621362 stop gained C/T snv 6.0E-05 2.1E-05 8