Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
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
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 6
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
rs11611206
LOC105369818 ; MDM1
0.851 0.200 12 68274666 intron variant G/A snv 0.15 4
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs11250144
BLK
0.925 0.200 8 11528767 intron variant G/A;C snv 2
rs12885526
TSHR ; LOC101928462
0.925 0.160 14 81108085 intron variant G/A snv 0.63 2
rs2267873
DIO2
0.925 0.160 14 80207471 intron variant A/G snv 0.20 2
rs1003199
IL12B
1.000 0.160 5 159328558 intron variant C/T snv 0.43 1
rs1264439
ABCF1 ; MIR877
1.000 0.160 6 30584725 intron variant A/C snv 0.74 1
rs1378228
DDAH1
1.000 0.160 1 85570890 intron variant G/C;T snv 1
rs287084
PDZRN4
1.000 0.160 12 41550605 intron variant T/C snv 1
rs6682848
DDAH1
1.000 0.160 1 85572793 intron variant A/C snv 0.89 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22