Disease: Lupus Erythematosus, Systemic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3117103
TSBP1-AS1
0.925 0.120 6 32381780 intron variant A/T snv 9.6E-02 2
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs3129939
TSBP1-AS1 ; TSBP1
0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs3129943
TSBP1-AS1 ; TSBP1
0.851 0.240 6 32370918 intron variant A/G snv 0.26 4
rs3130320
TSBP1-AS1
0.851 0.160 6 32255481 intron variant T/C snv 0.68 5
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 5
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs3134945
RNF5 ; MIR6833 ; AGPAT1
0.827 0.240 6 32178715 intron variant C/A snv 0.18 6
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs340630
AFF1
0.925 0.120 4 87037243 intron variant G/A snv 0.42 2
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 3
rs3761847
TRAF1
0.827 0.200 9 120927961 intron variant G/A snv 0.52 8
rs3766379
CD244
0.851 0.320 1 160837925 intron variant T/C snv 0.57 4
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs4958880
TNIP1
0.851 0.160 5 151058916 intron variant C/A;G snv 4
rs5029924
TNFAIP3 ; WAKMAR2
0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs5029937
TNFAIP3
0.882 0.160 6 137874014 intron variant G/T snv 0.13 4
rs540386
TRAF6
0.851 0.200 11 36503743 intron variant C/G;T snv 4
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25