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: rs6499640
rs6499640
FTO
7 0.925 0.160 16 53735765 intron variant G/A snv 0.59 0.800 1.000 1 2009 2009
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.800 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: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs7187961
rs7187961
FTO
2 16 53792122 intron variant T/C snv 0.86 0.700 1.000 1 2017 2017
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2007 2007