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 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1