Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4240384 1.000 0.120 5 124955709 intron variant T/C snv 0.85 1
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs3806932 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 3
rs1986734 1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs3806933 0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 7
rs2000260 1.000 0.120 1 108130783 downstream gene variant A/G snv 0.37 1
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs167769 0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 5
rs11495981 1.000 0.120 7 28137682 intron variant C/T snv 0.29 2
rs9399137 0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs3815700 1.000 0.120 19 32602346 intron variant T/C snv 0.19 1
rs2075277 1.000 0.120 22 21028193 3 prime UTR variant T/C snv 0.19 1
rs8041227 1.000 0.120 15 31246339 intergenic variant G/A snv 0.18 1
rs3744790 1.000 0.120 17 78897053 intron variant C/T snv 0.14 1
rs10062929 1.000 0.120 5 111072481 intron variant C/A snv 0.13 1
rs11819199 1.000 0.120 10 20576228 intergenic variant A/G snv 0.12 1
rs28530674 1.000 0.120 1 18907640 3 prime UTR variant A/G snv 0.11 1
rs8008716 1.000 0.120 14 26656559 intron variant A/G snv 8.9E-02 1
rs11206830 1.000 0.120 1 56494451 intron variant C/T snv 8.7E-02 1
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs599707 0.925 0.200 6 31840659 downstream gene variant C/T snv 7.6E-02 2
rs6736278 1.000 0.120 2 31220009 intron variant C/T snv 5.4E-02 1
rs149864795 1.000 0.120 2 31179541 intron variant G/A snv 4.8E-02 1
rs9956738
DCC
1.000 0.120 18 52414603 intron variant A/G snv 4.6E-02 1
rs17004598 1.000 0.120 21 43658675 intron variant T/G snv 4.5E-02 1