Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 19
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 12
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 9
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 8
rs63750875 0.742 0.280 2 47475171 missense variant G/A;C snv 1.6E-05 6
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 4
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 3
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 3
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 2
rs1057519725 0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 2
rs121913314
SRC
0.851 0.120 20 37403359 stop gained C/T snv 2
rs1131691029 0.827 0.160 17 7673794 missense variant C/G snv 2
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 1
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 1
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 1
rs121913538 0.882 0.080 12 25245328 missense variant C/A;G snv 1
rs1057519822 0.925 0.080 15 66481818 missense variant T/A snv 1