Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7789162 7 44833301 intron variant T/C snv 0.48 3
rs12155039 7 44833526 intron variant C/A;T snv 2
rs12155038 7 44833378 intron variant G/A snv 0.40 1
rs10267576 7 44831334 intron variant T/C snv 0.35 1