Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 6
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs1217393
AP4B1-AS1
0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs1635852
JAZF1
0.882 0.160 7 28149792 intron variant T/C snv 0.42 4
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs76246107
PRR12
0.851 0.160 19 49618017 intron variant G/A snv 7.7E-02 4
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 4
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 3
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs11893432
STAT4
0.827 0.120 2 191057148 intron variant C/G snv 0.21 3
rs77583790
IL12A-AS1
0.882 0.080 3 159976265 intron variant G/A;C snv 3
rs9373839
ATG5
0.882 0.080 6 106207742 intron variant T/C snv 0.15 3