Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13