Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10498633 0.925 0.080 14 92460608 intron variant G/T snv 0.19 1
rs12590654 1.000 0.080 14 92472511 intron variant G/A;T snv 1
rs12881735 1.000 0.080 14 92466484 intron variant T/C snv 0.19 1
rs8008388 1.000 0.080 14 92470346 intron variant G/A snv 0.69 1