Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2066847 0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 18
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1202989817 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18