Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35188965 5 1104823 intron variant C/G;T snv 12
rs150813342 9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9