Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs11234027 0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7944926 0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17