Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs2904880
CD19 ; RABEP2
1.000 0.040 16 28933075 missense variant C/G snv 0.72 0.76 2
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 2
rs3894194
GSDMA
0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 2
rs7774954
HLA-DQB2
0.925 0.120 6 32756412 3 prime UTR variant C/A;T snv 5.9E-02 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs11860650
ITGAM
0.882 0.120 16 31315385 intron variant C/T snv 0.14 2
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39 2
rs4963128
PHRF1
0.882 0.120 11 589564 intron variant T/C snv 0.64 2
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 2
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25 2
rs2239689
TNXB
0.925 0.120 6 32062507 intron variant G/A snv 0.33 0.25 2
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 1
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 1
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1