Disease: Body mass index procedure
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 4
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 4
rs10150332
NRXN3
14 79470621 intron variant T/C snv 0.26 3
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 3
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 3