rs4903961, TSHR

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.925 0.120 14 80996305 intron variant C/G snv 0.39 0.010 1.000 1 2017 2017
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.925 0.120 14 80996305 intron variant C/G snv 0.39 0.010 1.000 1 2017 2017