Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 3
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs11860650
ITGAM
0.882 0.120 16 31315385 intron variant C/T snv 0.14 2
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 2
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 2
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 2
rs2071295
TNXB
0.925 0.120 6 32070923 intron variant C/T snv 0.25 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 2