Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs137853011 0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 10
rs1800747 0.882 0.200 17 43063952 splice acceptor variant C/A;G;T snv 5
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 5
rs28904921 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 7
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 15
rs41293465 0.851 0.200 17 43045767 stop gained G/A snv 1.2E-05 6
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 6
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs80356923 0.882 0.200 17 43091891 stop gained C/A;T snv 9.9E-05 5
rs80356962 0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs80356978 0.827 0.200 17 43092809 stop gained C/A;T snv 7
rs80357123 0.827 0.200 17 43057078 stop gained G/A;C;T snv 1.2E-05 7
rs80357382 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 7
rs80358044 0.827 0.200 17 43074330 splice donor variant C/A;G;T snv 7
rs80358427 0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10