Source: GWASDB ×
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: rs9930506
rs9930506
FTO
5 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.760 0.857 1 2008 2018
dbSNP: rs3751812
rs3751812
FTO
4 0.882 0.160 16 53784548 intron variant G/T snv 0.30 0.730 1.000 1 2011 2017
dbSNP: rs4783819
rs4783819
FTO
2 0.925 0.120 16 53782735 intron variant G/C snv 0.68 0.710 1.000 1 2011 2014
dbSNP: rs7206790
rs7206790
FTO
2 0.925 0.160 16 53763996 intron variant C/G snv 0.49 0.710 1.000 1 2011 2014
dbSNP: rs8044769
rs8044769
FTO
3 0.851 0.200 16 53805223 intron variant T/A;C;G snv 0.710 1.000 1 2011 2018
dbSNP: rs8057044
rs8057044
FTO
2 0.882 0.080 16 53778702 intron variant G/A snv 0.54 0.710 1.000 1 2011 2019
dbSNP: rs9928094
rs9928094
FTO
2 1.000 0.080 16 53765993 intron variant A/G snv 0.42 0.710 1.000 1 2011 2013
dbSNP: rs9930333
rs9930333
FTO
2 0.882 0.120 16 53766065 intron variant T/C;G snv 0.710 1.000 1 2011 2013
dbSNP: rs10852521
rs10852521
FTO
2 1.000 0.080 16 53771053 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11075986
rs11075986
FTO
1 1.000 0.080 16 53771432 intron variant C/G snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs11075987
rs11075987
FTO
2 1.000 0.080 16 53781249 intron variant T/A;G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs11075989
rs11075989
FTO
3 0.925 0.120 16 53785965 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11642841
rs11642841
FTO
3 0.925 0.120 16 53811575 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs12149832
rs12149832
FTO
4 0.851 0.120 16 53808996 intron variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs12446228
rs12446228
FTO
2 1.000 0.080 16 53766475 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs13333228
rs13333228
FTO
1 1.000 0.080 16 53759886 intron variant T/C snv 0.74 0.700 1.000 1 2013 2013
dbSNP: rs1477196
rs1477196
FTO
2 0.851 0.200 16 53774346 intron variant A/G snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs17817288
rs17817288
FTO
2 1.000 0.080 16 53773852 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1861866
rs1861866
FTO
2 1.000 0.080 16 53770428 intron variant C/T snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs1861867
rs1861867
FTO
1 1.000 0.080 16 53814649 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs2058908
rs2058908
FTO
2 1.000 0.080 16 53772233 intron variant T/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs3751813
rs3751813
FTO
2 1.000 0.080 16 53784796 intron variant G/T snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs4784323
rs4784323
FTO
1 1.000 0.080 16 53763653 intron variant A/C;G snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs7190492
rs7190492
FTO
3 1.000 0.080 16 53794840 intron variant A/G snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs7201850
rs7201850
FTO
2 1.000 0.080 16 53787950 intron variant C/T snv 0.45 0.700 1.000 1 2011 2011