Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3753793
CCN1 ; DDAH1
0.851 0.240 1 85580205 upstream gene variant A/C snv 0.26 4
rs1264439
ABCF1 ; MIR877
1.000 0.160 6 30584725 intron variant A/C snv 0.74 1
rs6682848
DDAH1
1.000 0.160 1 85572793 intron variant A/C snv 0.89 1
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs11652878
ITGAE
0.925 0.160 17 3751686 missense variant A/C;G snv 4.0E-06; 0.12 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs2267873
DIO2
0.925 0.160 14 80207471 intron variant A/G snv 0.20 2
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 7
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 6
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29 10
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs40401
IL3 ; LOC105379174
0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33 8
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs1061501
IRF7
0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4