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
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs1554286 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs3024498 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7