Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs13023194 0.925 0.120 2 27744393 intergenic variant G/A;C snv 4
rs13404446 0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs17762454 0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs4665965 0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs780110 0.925 0.120 2 27462521 intron variant G/A snv 0.56 4