Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12938 0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs1518110 0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs1048971
CR2
0.851 0.160 1 207472977 synonymous variant G/A;T snv 0.34; 8.0E-06 4
rs1206255976 0.851 0.160 1 22637618 start lost T/G snv 7.0E-06 4
rs13023380 0.851 0.160 2 162297853 intron variant G/A snv 0.35 4
rs1876453
CR2
0.851 0.160 1 207454573 intron variant G/A snv 8.4E-02 4
rs3093061
CRP
0.851 0.160 1 159715192 upstream gene variant T/C snv 4.8E-02 4
rs370504038 0.851 0.160 3 48467569 missense variant A/G snv 1.2E-04 1.2E-04 4
rs10489265 0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs2070197 0.827 0.280 7 128948946 3 prime UTR variant T/C snv 9.0E-02 6
rs3813946
CR2
0.827 0.280 1 207454348 5 prime UTR variant T/C snv 0.16 5
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs1678542 0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs12583006 0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs292001 0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs1341239 0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs72556554 0.776 0.400 3 48466996 missense variant G/A;C snv 2.1E-04; 2.7E-04 9
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19