Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9653442 1.000 0.120 2 100208905 intron variant C/T snv 0.46 2
rs10865035 1.000 0.080 2 100219272 intron variant A/G snv 0.42 1
rs13010010 2 100236272 intron variant C/T snv 0.27 1