Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs7501939 0.776 0.280 17 37741165 intron variant C/T snv 0.41 4
rs3744763 0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 3
rs11263763 0.882 0.200 17 37743574 intron variant A/G snv 0.43 2
rs11651052 0.851 0.200 17 37742390 intron variant G/A snv 0.50 2
rs11651755 0.763 0.160 17 37739849 intron variant T/C snv 0.52 2
rs10908278 0.925 0.160 17 37739961 intron variant A/C;T snv 1