Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 9