Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12