Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs569550 0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs1973765 1.000 0.080 11 1877434 intron variant T/C snv 0.37 3
rs3817198 0.790 0.280 11 1887776 intron variant T/C snv 0.26 3
rs592373 0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 3
rs4980383 1.000 0.080 11 1880867 non coding transcript exon variant C/T snv 0.37 1