rs17545038, TSHR

N. diseases: 1
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 1.000 0.120 14 80991228 intron variant T/C snv 0.20 0.700 1.000 1 2011 2011