Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs12243326 0.925 0.160 10 113029056 intron variant T/C snv 0.27 1