Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913322 0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs185229225 0.851 0.120 4 13607505 intron variant T/C snv 4
rs121964872 0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3