Disease: Graves Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs1991517
LOC101928462 ; TSHR
0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs10004195
TLR10
0.790 0.320 4 38783103 upstream gene variant T/A snv 0.29 8
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs3792876
SLC22A4
0.790 0.280 5 132301616 intron variant C/T snv 6.9E-02 7
rs4794067
TBX21
0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 6
rs111033243
SLC26A4
0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs11675434
TPO
0.827 0.240 2 1404043 non coding transcript exon variant C/T snv 0.39 5
rs17250932
TBX21
0.851 0.160 17 47731941 upstream gene variant T/C snv 0.16 5
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs2076740
TG
0.827 0.160 8 132971813 missense variant C/T snv 0.31 0.37 5
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs2270450
LOC101926934 ; SLC25A27
0.827 0.200 6 46677138 3 prime UTR variant C/T snv 0.29 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 5
rs1061501
IRF7
0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 4
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs2563298
TMCO6 ; CD14
0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26 4