Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.100 0.750 12 2009 2018
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.030 1.000 3 2008 2019
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.030 1.000 3 2015 2018
dbSNP: rs1588413
rs1588413
FTO
3 0.882 0.200 16 54115620 3 prime UTR variant G/A snv 0.14 0.010 1.000 1 2018 2018
dbSNP: rs79206939
rs79206939
FTO
3 0.925 0.160 16 53826140 missense variant G/A snv 2.1E-03 6.4E-04 0.010 1.000 1 2018 2018
dbSNP: rs9926289
rs9926289
FTO
5 0.882 0.160 16 53786591 intron variant G/A snv 0.41 0.010 1.000 1 2018 2018
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2018 2018