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
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 3
rs2741045
UGT1A10 ; UGT1A8 ; UGT1A9
2 233671494 intron variant C/T snv 0.22 3
rs4148323
UGT1A10 ; UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A4
0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3
rs9274407
HLA-DQB1
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 2
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs17036170
PPARG
1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02 1