Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs12243326 0.925 0.160 10 113029056 intron variant T/C snv 0.27 3
rs17747324 0.925 0.160 10 112992744 intron variant T/C snv 0.17 3
rs12772424 1.000 0.040 10 113120792 intron variant A/T snv 0.57 2
rs290475 1.000 0.040 10 113114260 intron variant C/A;T snv 2
rs35198068 10 112995025 intron variant T/C snv 0.29 2
rs4132670 1.000 0.080 10 113008012 intron variant G/A snv 0.39 1