Disease: Graves Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs1534422
MIR3681HG
0.827 0.160 2 12500615 intron variant G/A snv 0.52 4
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 4