Disease: Body mass index procedure
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 4