Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
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
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5