Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs2934971 0.925 0.080 17 39698254 intron variant G/T snv 0.66 2
rs2643194 0.925 0.080 17 39696795 5 prime UTR variant C/T snv 0.67 2