Disease: Body Weight
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 7
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs29941 1.000 0.080 19 33818627 downstream gene variant A/G snv 0.70 6
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 5