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: rs3751812
rs3751812
FTO
8 0.882 0.160 16 53784548 intron variant G/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs55872725
rs55872725
FTO
6 16 53775211 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.700 1.000 1 2017 2017
dbSNP: rs9930333
rs9930333
FTO
7 0.882 0.120 16 53766065 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs9941349
rs9941349
FTO
6 1.000 0.080 16 53791576 intron variant C/T snv 0.34 0.700 1.000 1 2017 2017