Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258 12 111280427 intron variant C/A;T snv 24
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9