Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs6812193 0.882 0.080 4 76277833 intron variant C/T snv 0.38 3