Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs2812208 13 50132951 intron variant G/A;C snv 5
rs12513481 5 78155004 intron variant G/C snv 0.19 3