Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3800229 1.000 0.040 6 108675760 intron variant G/T snv 0.54 3
rs12206094 6 108584997 intron variant C/T snv 0.31 2
rs9400239 1.000 6 108656460 5 prime UTR variant T/C snv 0.55 2
rs2253310 6 108567390 intron variant C/G;T snv 1
rs3800230 6 108676925 intron variant T/G snv 0.15 1