Disease: Graves Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17879469
HLA-DRB1
0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs180223
TG
0.925 0.120 8 132888007 missense variant T/A;C;G snv 8.0E-06; 4.0E-06; 0.58 2
rs2071403
TPO
0.925 0.120 2 1413472 5 prime UTR variant A/G;T snv 2
rs2160322
MAGI2
0.851 0.160 7 78462650 intron variant G/A;C snv 5
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs327463
CEP128
0.925 0.120 14 80784911 missense variant T/C;G snv 0.38; 4.1E-06 2
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs3816769
STAT3
0.851 0.240 17 42346255 intron variant T/A;C snv 4
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs2291282
STAT3
0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 3
rs111033243
SLC26A4
0.827 0.400 7 107689112 missense variant T/C snv 6.1E-04 8.1E-04 5
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs3792876
SLC22A4
0.790 0.280 5 132301616 intron variant C/T snv 6.9E-02 7
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32