Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9404576 0.882 0.160 6 104736765 intron variant T/A;G snv 3
rs2499663 1.000 0.040 6 104852695 intron variant C/T snv 0.43 1
rs4079063 1.000 0.040 6 104818243 intron variant A/G;T snv 1
rs4336470 1.000 0.040 6 104732910 intron variant C/T snv 0.45 1