Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205