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: rs12920255
rs12920255
FTO
1 16 53898001 intron variant C/T snv 7.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs17817449
rs17817449
FTO
3 0.716 0.560 16 53779455 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs2072518
rs2072518
FTO
1 16 54118818 3 prime UTR variant A/G snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs62034143
rs62034143
FTO
1 16 54114716 3 prime UTR variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7185735
rs7185735
FTO
4 0.925 0.120 16 53788739 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7193144
rs7193144
FTO
1 0.925 0.120 16 53776774 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs8043757
rs8043757
FTO
3 0.925 0.120 16 53779538 intron variant A/T snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs9302652
rs9302652
FTO
2 1.000 0.080 16 53832063 intron variant C/T snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs9937053
rs9937053
FTO
1 0.882 0.160 16 53765595 intron variant G/A snv 0.42 0.700 1.000 1 2019 2019