Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1264622
HLA-L ; HCG18 ; HCG17
1.000 0.120 6 30289159 non coding transcript exon variant C/T snv 0.13 1
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 1
rs1265758
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32355752 intron variant A/G snv 0.51 1
rs1265759
TSBP1 ; TSBP1-AS1
1.000 0.120 6 32354616 intron variant C/T snv 0.47 1
rs1265761
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32353820 intron variant A/G;T snv 1
rs12679857
COLEC10
1.000 0.120 8 118965098 intergenic variant A/G snv 0.36 1
rs12908309
LINC02694
1.000 0.120 15 38636476 intron variant G/A snv 0.22 1
rs12923849
CLEC16A
1.000 0.120 16 10968140 intron variant G/A snv 0.13 1
rs12931878
CLEC16A
1.000 0.120 16 10948337 intron variant A/G snv 0.14 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 1
rs1367728
HLA-DPA1
1.000 0.120 6 33067038 non coding transcript exon variant G/A snv 0.10 1
rs148735424 1.000 0.120 6 32697982 intergenic variant -/TTCGTC;TTCGTCAGAC delins 1
rs154978 1.000 0.120 6 32931519 downstream gene variant C/T snv 0.54 1
rs1573649
HLA-DQB2
1.000 0.120 6 32763481 5 prime UTR variant G/A;C snv 0.56 1
rs163061
AQP4-AS1
1.000 0.120 18 26893778 intron variant G/C snv 0.68 1
rs1634731
MUC21
1.000 0.120 6 30987904 intron variant G/A snv 0.86 1
rs1634747
HLA-B
1.000 0.120 6 31314099 intron variant G/A snv 0.41 1
rs16956936
DNAH2
1.000 0.120 17 7730374 intron variant C/A;T snv 1
rs17208888 1.000 0.120 6 32411729 upstream gene variant G/A snv 8.0E-02 1
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16 1
rs17500468
HLA-DQA2
1.000 0.120 6 32743401 intron variant A/G snv 9.8E-02 1
rs188245 1.000 0.120 6 32988199 regulatory region variant A/G snv 0.44 1
rs1977090 1.000 0.120 6 33217801 downstream gene variant C/T snv 0.11 1
rs206769 1.000 0.120 6 32993327 regulatory region variant C/T snv 0.20 1
rs206777 1.000 0.120 6 32984769 downstream gene variant G/A snv 0.66 1