Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1092913 0.925 0.080 5 10467590 intron variant G/A snv 0.19 3