Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2869967 0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs7671167 0.925 0.040 4 88962828 intron variant C/T snv 0.53 4
rs1903003 0.925 0.080 4 88965146 intron variant C/G;T snv 3
rs2904259 4 88964563 intron variant T/A;C snv 3
rs2045517 4 88949813 intron variant C/T snv 0.49 3
rs2869966 1.000 0.040 4 88947927 intron variant C/T snv 0.47 3
rs2609255 0.882 0.080 4 88890044 intron variant G/T snv 0.73 1