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
rs7749323 0.925 0.200 6 137909252 intergenic variant G/A snv 3.3E-02 1
rs1422673
TNIP1
0.925 0.160 5 151059427 intron variant C/G;T snv 2
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 1
rs3792785
TNIP1
1.000 0.120 5 151072089 intron variant T/C snv 0.13 1
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 1
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
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 3
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 4
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs2844657 0.882 0.240 6 30861745 upstream gene variant A/G snv 0.17 3
rs4678
VARS2
0.925 0.200 6 30926164 missense variant G/A snv 0.14 0.15 2