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: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.800 1.000 3 2009 2017
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.800 1.000 2 2009 2019
dbSNP: rs10852521
rs10852521
FTO
2 1.000 0.080 16 53771053 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11075985
rs11075985
FTO
3 1.000 0.080 16 53771295 intron variant C/A snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs11075987
rs11075987
FTO
2 1.000 0.080 16 53781249 intron variant T/A;G snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs11075989
rs11075989
FTO
3 0.925 0.120 16 53785965 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11075990
rs11075990
FTO
6 0.925 0.120 16 53785981 intron variant A/G snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs113191842
rs113191842
FTO
5 16 53783406 intron variant G/A snv 9.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs11642841
rs11642841
FTO
3 0.925 0.120 16 53811575 intron variant C/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs12149832
rs12149832
FTO
8 0.851 0.120 16 53808996 intron variant G/A snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs12446228
rs12446228
FTO
2 1.000 0.080 16 53766475 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1477196
rs1477196
FTO
7 0.851 0.200 16 53774346 intron variant A/G snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs17817288
rs17817288
FTO
3 1.000 0.080 16 53773852 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs17817964
rs17817964
FTO
6 0.925 0.120 16 53794154 intron variant C/T snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs1861866
rs1861866
FTO
2 1.000 0.080 16 53770428 intron variant C/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs2058908
rs2058908
FTO
2 1.000 0.080 16 53772233 intron variant T/C snv 0.79 0.700 1.000 1 2009 2009
dbSNP: rs3751812
rs3751812
FTO
8 0.882 0.160 16 53784548 intron variant G/T snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs3751813
rs3751813
FTO
2 1.000 0.080 16 53784796 intron variant G/T snv 0.54 0.700 1.000 1 2009 2009
dbSNP: rs4783819
rs4783819
FTO
3 0.925 0.120 16 53782735 intron variant G/C snv 0.68 0.700 1.000 1 2009 2009
dbSNP: rs7185735
rs7185735
FTO
5 0.925 0.120 16 53788739 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs7190492
rs7190492
FTO
3 1.000 0.080 16 53794840 intron variant A/G snv 0.68 0.700 1.000 1 2009 2009
dbSNP: rs7193144
rs7193144
FTO
6 0.925 0.120 16 53776774 intron variant T/C snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs7201850
rs7201850
FTO
2 1.000 0.080 16 53787950 intron variant C/T snv 0.45 0.700 1.000 1 2009 2009