Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1924981 1.000 0.040 13 28448508 intron variant C/T snv 0.32 1
rs9319428 0.925 0.080 13 28399484 intron variant G/A snv 0.30 1
rs9508025 0.925 0.040 13 28409926 intron variant C/G;T snv 1
rs9513112 1.000 0.040 13 28423565 intron variant G/A snv 0.30 1