Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 4
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 3
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 3
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 3
rs3117222
HLA-DPA2
0.882 0.280 6 33093172 intron variant C/T snv 0.33 3
rs4938573 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 2
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2
rs9275517
MTCO3P1
0.925 0.200 6 32706872 non coding transcript exon variant A/G snv 0.58 2
rs13198610 1.000 0.120 6 32457895 downstream gene variant G/T snv 0.13 1
rs28895078 1.000 0.120 6 32450114 intergenic variant C/A;G snv 0.13 1
rs28895103 1.000 0.120 6 32451687 intergenic variant G/A snv 0.13 1
rs28895171 1.000 0.120 6 32455244 downstream gene variant G/A snv 0.13 1
rs28895187 1.000 0.120 6 32456603 downstream gene variant G/A snv 0.13 1
rs3115667 0.882 0.200 6 31675622 downstream gene variant T/A;C snv 0.74 1
rs35571839 1.000 0.120 6 32544836 intergenic variant C/T snv 0.11 1
rs35998847 1.000 0.120 6 32699220 intergenic variant G/A snv 0.14 1
rs2857597
AIF1
0.882 0.200 6 31617223 upstream gene variant T/A snv 0.74 1
rs9274614
HLA-DQB1
1.000 0.120 6 32668069 intron variant C/A;G snv 1
rs28605404
HLA-DRB1
1.000 0.120 6 32601910 intergenic variant A/G snv 0.10 1