Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
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
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
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
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
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
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
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
rs3753793
CCN1 ; DDAH1
0.851 0.240 1 85580205 upstream gene variant A/C snv 0.26 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
rs11083522
MIR4530 ; PLEKHG2
1.000 0.160 19 39410971 upstream gene variant T/C snv 0.32 1