Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894060 0.882 0.120 8 1780316 missense variant C/T snv 3.2E-05 7.0E-06 3
rs104894064 0.882 0.120 8 1771124 missense variant C/G;T snv 1.0E-04; 2.4E-05 3
rs104894385 0.925 0.120 13 76992176 stop gained G/A;T snv 2.7E-05; 3.1E-05 2
rs104894386 0.925 0.120 13 76995077 missense variant G/A;C snv 8.0E-06 2
rs104894483 0.925 0.120 15 68214373 stop gained C/A;G;T snv 6.8E-05; 2.6E-03; 2.0E-05; 4.0E-06 3
rs1057516677 0.925 0.120 16 28477875 stop gained G/T snv 2
rs1060502179 1.000 0.120 11 6618823 missense variant A/C snv 7.0E-06 1
rs113019349 0.925 0.120 11 6616004 splice donor variant C/G;T snv 2
rs119455954 0.925 0.120 11 6616056 missense variant C/T snv 1.6E-05 4.9E-05 2
rs119455955 0.851 0.120 11 6617040 stop gained G/A snv 2.2E-04 2.4E-04 4
rs119455957 0.882 0.120 11 6616696 missense variant C/A snv 8.0E-06 7.0E-06 3
rs121434286 0.882 0.120 16 28482500 stop gained C/A;T snv 2.4E-05 3
rs121908080 0.925 0.120 15 68211698 inframe deletion ATG/- delins 2
rs121908199 0.925 0.120 11 6615542 missense variant C/T snv 2
rs121908200 0.925 0.120 11 6615442 missense variant C/G snv 2.0E-05 2.1E-05 2
rs121908202 0.925 0.120 11 6615172 missense variant G/A snv 2.4E-05 2
rs121908209 0.925 0.120 11 6617045 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs1267314028 1.000 0.120 16 28486388 synonymous variant G/A snv 1
rs137852695 0.925 0.120 1 40091398 missense variant T/A snv 7.0E-04 6.0E-04 4
rs137852696 0.882 0.120 1 40092409 missense variant T/G snv 1.6E-05 5.6E-05 3
rs137852700 0.851 0.120 1 40089495 stop gained G/A;C snv 2.4E-04; 1.2E-05 4
rs140948465 0.925 0.120 4 127930800 missense variant G/A;T snv 4.0E-06; 8.0E-06 2
rs144495588 0.925 0.120 8 1771553 stop gained G/C;T snv 8.0E-06; 1.2E-05 2
rs154774640 0.925 0.120 15 68218584 stop gained G/C snv 8.0E-06 2.1E-05 2
rs1554902052 0.925 0.120 11 6617430 splice acceptor variant T/C snv 2