Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs3891175
HLA-DQB1
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20 3
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 2
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs2069763
IL2
0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29 1
rs11065904
SH2B3 ; ATXN2
0.882 0.080 12 111449163 3 prime UTR variant T/A snv 3.2E-02 1
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 1