Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs669408 1 232383404 regulatory region variant A/C snv 0.52 1
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 1