Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 5
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs9277341
HLA-DPA1
0.882 0.280 6 33071848 intron variant T/A;C snv 3
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 2
rs1949829 0.925 0.200 7 51470190 upstream gene variant C/T snv 0.12 1
rs26595 0.925 0.200 5 116423793 intergenic variant G/A;T snv 1
rs3117242 0.925 0.200 6 33102116 upstream gene variant A/G snv 0.34 1
rs595018
LOC105369322
0.925 0.200 11 60824803 upstream gene variant T/A;C snv 1