Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 13