Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs2498794 14 104778914 intron variant A/G snv 0.54 2