Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs987052 16 86288853 intron variant T/C snv 0.23 2