Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 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
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C 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
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs4130548
GIPC2 ; DNAJB4
1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5