Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 7
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 4
rs62104180 2 466003 intergenic variant G/A snv 2.9E-02 4
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 4
rs9813495
CADM2
3 85777231 intron variant A/G snv 0.15 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4