Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9275602 1.000 0.120 6 32715035 upstream gene variant C/A snv 0.13 1
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 3
rs9275595 0.925 0.200 6 32713578 upstream gene variant T/C snv 0.23 2
rs9275555 0.925 0.200 6 32709311 upstream gene variant C/T snv 0.24 2
rs9275408 1.000 0.120 6 32702333 downstream gene variant T/C snv 0.30 1
rs9275388 1.000 0.120 6 32701307 downstream gene variant T/C snv 0.30 1
rs9275383 1.000 0.120 6 32701069 regulatory region variant G/T snv 0.11 1
rs9275371 0.925 0.200 6 32700519 regulatory region variant T/C snv 0.29 2
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs9275313 1.000 0.120 6 32697982 intergenic variant G/T snv 9.9E-02 1
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9275184 0.882 0.200 6 32686937 regulatory region variant T/C snv 9.1E-02 3
rs9273349
HLA-DQB1-AS1
0.827 0.200 6 32658092 upstream gene variant T/C;G snv 1
rs927292
ZFP36L1
1.000 0.120 14 68792124 intron variant C/G snv 0.68 1
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 6
rs9271568 0.925 0.200 6 32622686 TF binding site variant G/A snv 0.27 2
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs9268831
HLA-DRB9
0.851 0.280 6 32459971 non coding transcript exon variant C/T snv 0.54 0.51 3
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs9268615 0.882 0.280 6 32435112 upstream gene variant G/A snv 0.38 3
rs9268542 0.851 0.280 6 32416944 intergenic variant A/G snv 0.35 3
rs9268530 0.925 0.200 6 32415446 regulatory region variant T/C snv 0.13 2
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 3
rs9268005
TSBP1-AS1
1.000 0.120 6 32256611 intron variant C/A;T snv 1
rs9267992 0.882 0.240 6 32252620 upstream gene variant G/A snv 0.89 3