Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs9270986
HLA-DRB1
0.882 0.160 6 32606283 intergenic variant A/C snv 0.85 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 4
rs3129963 0.851 0.280 6 32412431 downstream gene variant A/G snv 0.17 4
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 3
rs1634718
MUC22
0.925 0.160 6 31005088 regulatory region variant A/G snv 0.20 2
rs9277534
HLA-DPB1
0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 2
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 1
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs887464
POU5F1 ; PSORS1C3
0.925 0.200 6 31178143 intron variant C/A;T snv 2
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6