Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2745353 6 127131790 intron variant C/T snv 0.55 2
rs9491697 1.000 0.040 6 127134977 intron variant A/G snv 0.41 1
rs9491696 6 127131494 intron variant C/G snv 0.45 1
rs7745274 6 127188012 intron variant G/A snv 0.56 1
rs6569474 6 127172466 intron variant A/T snv 0.54 1