Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 1
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs9933507
CLEC16A
1.000 0.120 16 11107571 intron variant T/C snv 0.46 1
rs9924471
SGF29
1.000 0.120 16 28580209 intron variant G/A snv 0.16 1
rs9810233 0.925 0.200 3 105292046 intergenic variant A/G snv 0.25 1
rs9784758 0.925 0.200 6 32820734 intron variant T/C snv 0.11 2
rs9501626 0.925 0.200 6 32432567 regulatory region variant C/A snv 0.18 2
rs9501239 1.000 0.120 6 32927803 intergenic variant A/G snv 5.7E-02 1
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 4
rs941576
MEG3
1.000 0.120 14 100839708 intron variant A/G snv 0.45 1
rs9388489
CENPW
0.925 0.160 6 126377573 intron variant A/G;T snv 2
rs9378200 0.925 0.120 6 31605150 intergenic variant T/C snv 5.4E-02 5
rs9368741 1.000 0.120 6 32769730 intergenic variant G/A snv 0.30 1
rs9368699
SNHG32 ; SNORD48
0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs928815
LOC100287329 ; LTA
1.000 0.120 6 31563438 downstream gene variant T/G snv 0.65 1
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 5
rs9276991 0.882 0.240 6 33014071 upstream gene variant A/G snv 6.0E-02 3
rs9276831
PSMB9
1.000 0.120 6 32864256 downstream gene variant A/G snv 0.12 1
rs9276370
HLA-DQA2
0.882 0.200 6 32739518 upstream gene variant G/T snv 0.51 2
rs9276291 0.925 0.200 6 32735036 upstream gene variant T/A;C snv 2
rs9276162 0.882 0.280 6 32730680 downstream gene variant G/A snv 0.74 3
rs9275653
LOC102725019
1.000 0.120 6 32718088 non coding transcript exon variant G/A snv 0.60 1