Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs7996639
HS6ST3
13 96366836 intron variant G/A snv 0.50 3
rs11855017
MAPKBP1
15 41803948 intron variant C/A snv 0.15 2
rs12879423 14 25458626 intergenic variant A/G snv 0.55 2
rs1884429 1 11052779 downstream gene variant T/C snv 0.74 2
rs9843653 3 49883138 downstream gene variant T/A;C snv 2