Disease: Lupus Erythematosus, Systemic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12537
MTMR3 ; HORMAD2-AS1
0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13389408
STAT4
0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs1341239
PRL ; CASC15
0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17581834
IL19
0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs17860508
LOC285626
0.752 0.360 5 159333192 intron variant TTAGAG/GC delins 11
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121