Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2299383 1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs3802177 1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 4
rs11558471 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs1899951 0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs2246012 1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs329122 1.000 0.080 5 134528909 intron variant G/A snv 0.45 2
rs7570971 1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs5215 0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 3
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 5
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs2304130 1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 5