Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31