Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs1279683 1.000 0.040 20 5002446 intron variant G/A;C snv 3
rs2072153 17 49312652 intron variant G/A;C snv 3.7E-04; 0.33 3
rs115560420 3 67375539 3 prime UTR variant G/T snv 8.8E-02 2
rs4894797 3 172065756 intron variant G/A snv 0.47 2
rs6121246 20 31845549 5 prime UTR variant C/T snv 0.20 0.29 2