Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 52
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33
rs1801155
APC
0.657 0.393 5 112839514 missense variant T/A snp 2.0E-03; 8.0E-06 6.4E-04 31
rs1801278 0.652 0.393 2 226795828 missense variant C/G,T snp 4.0E-06; 5.2E-02 6.0E-02 29
rs1045485 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 26
rs121913286 0.679 0.250 3 179218306 missense variant C/A,G snp 21
rs752021744 0.699 0.429 3 138759306 T/C snp 1.2E-05 21
rs1799977 0.679 0.357 3 37012077 missense variant A/C,G,T snp 0.23 0.23 20
rs2854744 0.707 0.357 7 45921476 intron variant G/T snp 0.48 15
rs1950902 0.756 0.214 14 64415662 missense variant A/G snp 0.83 0.81 10
rs459552
APC
0.756 0.286 5 112841059 missense variant T/A,G snp 0.79 0.81 10
rs8176318 0.821 0.179 17 43045257 3 prime UTR variant C/A snp 0.34 0.30 5