Disease: Autoimmune Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 7
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs13447
NCF1C
0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26