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: rs11075992
rs11075992
FTO
3 1.000 0.080 16 53786154 intron variant T/C snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.030 1.000 3 2011 2014
dbSNP: rs12597786
rs12597786
FTO
1 1.000 0.080 16 53787395 intron variant C/T snv 3.2E-02 0.010 1.000 1 2013 2013
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs7204609
rs7204609
FTO
6 0.827 0.200 16 53799693 intron variant T/C snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs8062891
rs8062891
1 1.000 0.080 16 54055160 intron variant T/C snv 0.80 0.010 1.000 1 2013 2013