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: rs8050136
rs8050136
FTO
9 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.900 0.964 4 2007 2019
dbSNP: rs9939609
rs9939609
FTO
18 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.900 0.961 2 2007 2019
dbSNP: rs11642841
rs11642841
FTO
1 0.925 0.120 16 53811575 intron variant C/A;G snv 0.810 1.000 1 2010 2014
dbSNP: rs9936385
rs9936385
FTO
3 0.925 0.120 16 53785257 intron variant T/C snv 0.41 0.800 1.000 3 2012 2016
dbSNP: rs7185735
rs7185735
FTO
4 0.925 0.120 16 53788739 intron variant A/G;T snv 0.800 1.000 1 2011 2018
dbSNP: rs1421085
rs1421085
FTO
10 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.730 1.000 3 2009 2019