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: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs16952619
rs16952619
FTO
1 16 53884735 intron variant A/G snv 4.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs28567725
rs28567725
FTO
1 16 53792116 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs9930333
rs9930333
FTO
7 0.882 0.120 16 53766065 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016