Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs434082
SLC8A1
0.925 0.160 2 40257934 intron variant C/T snv 0.14 3
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs1108131
CAMK1D
0.925 0.160 10 12455748 intron variant T/C snv 0.28 2
rs11893826
SLC8A1
0.925 0.160 2 40337507 intron variant G/A snv 0.27 2