Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11205303 0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs3817428 15 88872016 missense variant C/G snv 0.20 0.20 3
rs481806 7 28167681 intron variant G/T snv 0.77 2