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
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 7
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 5
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 5
rs62048402
FTO
0.882 0.200 16 53769311 intron variant G/A snv 0.31 3
rs56077980
FTO
1.000 0.080 16 54107654 intron variant -/T delins 0.26 1