Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 1
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 1
rs2233287
TNIP1
0.925 0.160 5 151060536 intron variant G/A snv 0.11 2
rs3792783
TNIP1
0.882 0.280 5 151076171 intron variant A/G snv 0.25 1
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 1
rs3093024
LOC105378122 ; CCR6
0.882 0.200 6 167119305 non coding transcript exon variant A/G snv 0.61 1
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 1
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 2
rs3131917 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 1
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 1
rs704840
LOC100506023 ; TNFSF4
0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 1
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs7601754
STAT4
0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 1