Source: GWASCAT ×
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: rs9940128
rs9940128
FTO
3 0.851 0.120 16 53766842 intron variant G/A snv 0.42 0.700 1.000 2 2013 2019
dbSNP: rs12149832
rs12149832
FTO
3 0.851 0.120 16 53808996 intron variant G/A snv 0.31 0.700 1.000 2 2012 2019
dbSNP: rs7202116
rs7202116
FTO
1 0.882 0.120 16 53787703 intron variant A/G snv 0.41 0.700 1.000 2 2012 2019
dbSNP: rs1558902
rs1558902
FTO
12 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.700 1.000 11 2010 2019
dbSNP: rs8050136
rs8050136
FTO
9 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.800 1.000 5 2009 2019
dbSNP: rs6499640
rs6499640
FTO
2 0.925 0.160 16 53735765 intron variant G/A snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs1121980
rs1121980
FTO
5 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 3 2008 2019
dbSNP: rs9939609
rs9939609
FTO
18 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 6 2007 2019
dbSNP: rs9930506
rs9930506
FTO
3 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 2 2007 2019