Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6058227 20 35308144 intron variant C/T snv 0.15 2
rs6060369 20 35319358 intron variant T/C snv 0.49 1
rs6060373 0.925 0.200 20 35326405 intron variant A/G snv 0.49 1
rs6088792 20 35321981 intron variant C/T snv 0.26 1
rs6088813 20 35387378 intron variant C/A snv 0.54 1