Disease: Rheumatoid Arthritis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs9603612
COG6
0.925 0.120 13 39760715 intron variant C/G snv 0.30 2
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs58721818 0.851 0.160 6 137922602 regulatory region variant C/G;T snv 4
rs10954214
IRF5
0.851 0.160 7 128949579 3 prime UTR variant C/T snv 0.64 4
rs11085725
TYK2
0.851 0.160 19 10351837 intron variant C/T snv 0.24 4
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs5029924
TNFAIP3 ; WAKMAR2
0.851 0.200 6 137866361 intron variant C/T snv 0.13 2
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs1217393
AP4B1-AS1
0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs2422345
LOC100506023 ; TNFSF4
0.851 0.160 1 173368608 upstream gene variant G/A snv 0.63 4