Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4820323 22 38203760 non coding transcript exon variant C/A;G;T snv 4
rs133027 22 38179492 intron variant T/- delins 0.46 2
rs2277844 22 38181508 intron variant G/A snv 0.53 2
rs3761445 22 38199404 intron variant G/A snv 0.52 2
rs55951234 22 38205423 5 prime UTR variant -/CTC delins 2
rs5756931 22 38150026 non coding transcript exon variant T/A;C snv 1