Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 58
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs356182 0.882 0.080 4 89704960 intron variant G/A snv 0.65 3
rs356165 0.882 0.080 4 89725735 3 prime UTR variant G/A snv 0.54 3
rs10516846 1.000 0.080 4 89775184 intron variant A/G snv 3.9E-02 1