Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6443624 0.776 0.200 3 179179886 intron variant C/A snv 0.30 8
rs7621329 1.000 0.040 3 179157086 intron variant C/T snv 0.26 1
rs7640662 1.000 0.040 3 179184213 intron variant C/G snv 0.10 1