Disease: Juvenile-Onset Still Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10194635
LINC01104
0.807 0.120 2 100217755 intron variant T/A;G snv 6
rs27293
LNPEP
0.807 0.120 5 97021474 intron variant A/G;T snv 6
rs2847293 0.807 0.120 18 12782449 downstream gene variant A/G;T snv 6
rs3825568
ZFP36L1
0.807 0.120 14 68793871 5 prime UTR variant C/G;T snv 6
rs6946509 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 6
rs7127214
PRR5L
0.807 0.120 11 36322143 intron variant C/G;T snv 6
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs73300638
JAZF1
0.807 0.120 7 28147725 intron variant A/C;G snv 6
rs79575701
ZBTB7C
0.882 0.120 18 48053250 intron variant C/A;T snv 3
rs9532434
COG6
0.807 0.120 13 39781776 intron variant T/A;C snv 8
rs149850873
PTPN2
0.807 0.120 18 12885121 intron variant G/A snv 1.7E-02 6
rs45539732
STAT1
0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 6
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72632736 0.882 0.120 1 4389144 intergenic variant A/G snv 4.3E-02 3
rs114940806
KLF17
0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 3
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs7909519
IL2RA
0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 6
rs72698115
IL6R ; IL6R-AS1
0.807 0.120 1 154406893 intron variant A/C snv 7.2E-02 6
rs41291794 0.882 0.120 6 32457985 downstream gene variant A/T snv 7.5E-02 3
rs79893749
CCR3
0.807 0.120 3 46212159 intron variant C/T snv 0.10 6
rs12517545
LINC01331
0.882 0.120 5 74384489 intron variant G/A snv 0.13 3
rs11714843
TIMMDC1
0.807 0.120 3 119502217 intron variant T/A snv 0.15 6
rs10213692
ANKRD55
0.807 0.120 5 56146422 intron variant T/C snv 0.17 6
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 8