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
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs2657879 1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5