Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs261342 15 58438954 intron variant G/A;C;T snv 3
rs261334 15 58434545 intron variant G/C snv 0.73 3
rs588136 15 58438299 intron variant C/G;T snv 2
rs261336 15 58450219 intron variant G/A snv 0.81 1