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
rs17235416 0.807 0.200 2 218395091 3 prime UTR variant TGTG/- del 8.4E-02 6
rs17221959 0.882 0.160 2 218387907 synonymous variant C/T snv 7.0E-02 0.12 3
rs2279015 0.882 0.080 2 218394547 non coding transcript exon variant G/A snv 0.51 3