Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs2274273 0.882 0.120 14 55147918 downstream gene variant G/A snv 0.40 5