Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs368939818 0.763 0.280 11 49156734 missense variant G/A snv 4.0E-05 2.1E-05 13
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs755001634 0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13