Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3117222 0.882 0.280 6 33093172 intron variant C/T snv 0.33 3
rs2281388 0.851 0.400 6 33092341 non coding transcript exon variant G/A snv 2.6E-02 2
rs3128917 0.925 0.200 6 33092219 non coding transcript exon variant T/G snv 0.33 2
rs3117216 1.000 0.080 6 33095626 intron variant A/G snv 0.38 1