Disease: Rheumatoid Arthritis
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 7
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 3
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 3
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 3
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs13397
MIR3202-2 ; TMEM187
0.925 0.200 X 153982797 synonymous variant G/A snv 0.27 0.15 2
rs16867384
LINC01934
0.925 0.200 2 181246479 intron variant T/C snv 0.19 2
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 2
rs212400
LOC105378083
0.925 0.200 6 159052542 non coding transcript exon variant A/G snv 0.64 2
rs4073285
MMEL1
0.925 0.200 1 2608357 intron variant C/T snv 0.40 2
rs62323881 0.925 0.200 4 122117140 regulatory region variant C/A;T snv 2
rs6696533 0.925 0.200 1 198764438 intergenic variant T/C snv 0.28 2
rs6749371
STAT4
0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02 2
rs67676925
CCR3
0.925 0.200 3 46232768 intron variant T/C snv 5.5E-02 2