Disease: Lupus Erythematosus, Systemic
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 5
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14