Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs79105258 12 111280427 intron variant C/A;T snv 23
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7