Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758656 9 4852599 intron variant A/G snv 0.19 6
rs10758658 9 4856877 intron variant G/A snv 0.15 3
rs2236496 9 4844265 intron variant T/C snv 0.19 3
rs17803780 9 4849647 intron variant T/C snv 0.19 2
rs3824430 9 4847168 intron variant T/C snv 0.19 1