Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11