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
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs539703
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32320685 intron variant A/C;T snv 4
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 4
rs9268877
HLA-DRB9
0.827 0.200 6 32463370 intron variant A/G;T snv 4
rs3101942
LOC100294145
0.882 0.200 6 32902280 intergenic variant G/A;C snv 3
rs3130311 0.882 0.200 6 32249590 intergenic variant A/G;T snv 3
rs3134926 0.882 0.200 6 32232370 intergenic variant C/A;G snv 3
rs9267954 0.882 0.200 6 32245275 regulatory region variant A/C;T snv 3
rs9268560 0.882 0.200 6 32421735 intergenic variant C/G;T snv 3
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs16830359 1.000 0.080 1 43130713 intergenic variant G/A;T snv 2
rs7746922
HLA-DRB9
0.925 0.200 6 32463198 intron variant C/A;G;T snv 2
rs9272723
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.925 0.200 6 32641650 intron variant T/C snv 2
rs9276440
HLA-DQA2
0.925 0.120 6 32747006 3 prime UTR variant A/G;T snv 2
rs10032741 1.000 0.080 4 44958427 intergenic variant T/A;C snv 1
rs1011356 1.000 0.080 14 76678871 intron variant C/A;G snv 1
rs10226621
SDK1
1.000 0.080 7 4068008 intron variant A/C;G snv 1
rs10418441
COLGALT1
1.000 0.080 19 17569292 intron variant C/A;T snv 1
rs10490165
NRXN1
1.000 0.080 2 50961428 intron variant T/A;C snv 1
rs10775354
RBFOX1
1.000 0.080 16 6757689 intron variant A/C;T snv 1
rs10780661
SLC28A3
1.000 0.080 9 84311392 intron variant A/G;T snv 1