Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs4704220
CERT1
5 75461731 intron variant G/A snv 0.55 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
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
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4