Source: GWASCAT ×
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 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 5
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 4
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3