Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs80358920 0.732 0.400 13 32346841 stop gained C/G;T snv 12
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
rs80358427 0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 9
rs80358785 0.790 0.240 13 32340000 stop gained C/A;G snv 1.6E-05 9
rs80356962 0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs80359550 0.807 0.280 13 32340301 frameshift variant T/- del 1.8E-04 8
rs80359584 0.807 0.280 13 32340757 frameshift variant CTTAA/- delins 4.2E-06 1.4E-05 8
rs28904921 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 7
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
rs80357906 0.827 0.200 17 43057062 frameshift variant -/G delins 1.8E-04 7
rs80358044 0.827 0.200 17 43074330 splice donor variant C/A;G;T snv 7
rs80358981 0.827 0.200 13 32356550 stop gained C/T snv 2.0E-05 1.4E-05 7
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
rs80357783 0.851 0.200 17 43124030 frameshift variant -/T delins 4.0E-06 6