Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 2
rs2133189 0.925 0.040 1 222641100 intron variant C/T snv 0.56 1
rs2291832 1.000 0.040 1 222653139 intron variant G/A;C snv 0.64; 1.2E-05 1