rs12101261, 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 80984885 intron variant C/T snv 0.37 0.810 1.000 2 2011 2014