Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7916441 10 79165820 intron variant G/C snv 0.39 2
rs7926971 11 12676493 intron variant A/G snv 0.41 2
rs8067165 17 8128618 upstream gene variant C/A;G;T snv 3
rs9435733 1 16981759 intron variant T/C snv 0.41 3