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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs2075820 0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs1878672 0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs3024491 0.925 0.040 1 206771701 intron variant C/A;T snv 2