Disease: Graves Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 3
rs12101255
TSHR
0.925 0.120 14 80984708 intron variant C/T snv 0.37 2
rs1269486
GATA3 ; GATA3-AS1 ; LOC107984204
0.925 0.120 10 8054236 intron variant A/G snv 0.77 2
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 4
rs180223
TG
0.925 0.120 8 132888007 missense variant T/A;C;G snv 8.0E-06; 4.0E-06; 0.58 2
rs2071400
TPO
0.882 0.120 2 1412867 intron variant C/T snv 0.11 3
rs2071403
TPO
0.925 0.120 2 1413472 5 prime UTR variant A/G;T snv 2
rs2184658
HLX-AS1 ; HLX
0.925 0.120 1 220879115 intron variant C/G snv 0.20 2
rs2268458
TSHR
0.925 0.120 14 80996551 intron variant T/C snv 0.20 2
rs2291282
STAT3
0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 3
rs2569192
CD14 ; TMCO6
0.925 0.120 5 140635623 upstream gene variant G/C snv 0.27 2
rs308328
UNC93B1
0.925 0.120 11 67997585 non coding transcript exon variant T/C snv 0.54 2
rs327463
CEP128
0.925 0.120 14 80784911 missense variant T/C;G snv 0.38; 4.1E-06 2
rs3783938
TSHR ; LOC101928462
0.925 0.120 14 81128036 intron variant C/T snv 0.13 2
rs4411444
TSHR
0.925 0.120 14 80978764 intron variant A/G snv 0.43 2
rs4903961
TSHR
0.925 0.120 14 80996305 intron variant C/G snv 0.39 2
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs5998672
UBE2L3
0.925 0.120 22 21612153 intron variant G/A snv 0.31 2
rs7537605
VAV3
0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 6
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