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
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 5
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 2
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 1
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 1
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 1
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 1
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 1
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs11935941
LOC107986195
1.000 0.040 4 148731326 intron variant A/C snv 0.31 1
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 1