Disease: Body mass index
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 5
rs2650492
SBK1
16 28322090 3 prime UTR variant G/A snv 0.20 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5