Disease: Rheumatoid Arthritis
Source: GWASCAT ×
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 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs2451258
LOC112267968
0.807 0.160 6 159085568 intron variant C/T snv 0.75 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3