Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6918289 0.925 0.040 6 41134089 intron variant G/T snv 9.8E-02 2
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs74577862 0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs201989364 0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05 3
rs138227502 0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04 2
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs6903956 0.763 0.160 6 11774350 intron variant A/G snv 0.65 10
rs2269422 0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs2518136 0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs7217186 0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs12762303 0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs4076317 0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1264352930 0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs1384889210 0.827 0.040 11 116836193 missense variant C/A snv 5
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs200222843 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 4