Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 3
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs2647045 6 32700323 TF binding site variant G/A snv 0.27 1
rs4530903 6 32614112 intergenic variant C/T snv 0.10 1
rs9461776
HLA-DRB1
0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 1
rs2304240
ICAM3
0.882 0.200 19 10338716 synonymous variant A/G snv 0.81 0.85 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs707824
LOC101928354
0.925 0.120 6 14636732 intergenic variant T/C snv 0.74 1
rs6773854
LOC105374265
1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 1
rs273429
LOC105375763
8 131467654 intergenic variant C/T snv 0.43 1
rs12289961
OR10Q2P
11 58292720 non coding transcript exon variant C/T snv 0.28 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs948562
ZFP91-CNTF ; ZFP91
11 58580292 intron variant A/G snv 0.15 1