Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs2647046 0.882 0.200 6 32700559 TF binding site variant A/C snv 0.64 3
rs437179
SKIV2L ; CYP21A2
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78 3
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs2524095
LINC02571 ; HLA-B ; LOC112267902
0.925 0.160 6 31298340 intron variant A/C snv 0.65 2
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs4948088 0.925 0.160 7 50959497 intron variant A/C snv 0.96 2
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 2
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 2
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 2
rs12948909
CAVIN1
0.925 0.120 17 42418584 intron variant A/C snv 0.24 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs669607
LINC01967
1.000 0.080 3 28029953 intron variant A/C snv 0.38 1
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 2
rs1805755
KLRG1 ; M6PR
1.000 0.080 12 8949816 upstream gene variant A/C;G snv 1.7E-02 1
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 1
rs4285028
SLC15A2
1.000 0.080 3 121941817 3 prime UTR variant A/C;G snv 1
rs6896969 1.000 0.080 5 40424324 intron variant A/C;G snv 0.57 1
rs3134603
PPT2-EGFL8 ; PPT2
0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4